Project Role: Product Support Tech AdvisorExperience: 4-8 YearsJob Location: Bangalore (Hybrid)Skills: Python, SQL, NumPy, Panda, Django Roles and ResponsibilitiesTeam is involved in assessing & resolving issues/query raised (on Service-Now VIA platform) by product users and proactively work with product team (includes Product manager and development team) for timely resolution. Analyzing and identifying technical issues (both frontend & backend) reported by users and providing solution to the same, either through direct assistance or by guiding users through troubleshooting steps Team is also responsible for developing and maintaining a comprehensive knowledge base of FAQs and troubleshooting guides.Keeping documentation up-to-date based on new product releases, features etc Providing training sessions to help users understand and use the product effectively. Keeping users informed about knows issues, product updates and resolutions.Tracking Key performance indicators (KPIs) by publishing various product dashboards.Collaborating with Product users, dev teams, and other up/down stream applications for a unified customer experience.Regular connects with product managers/teams for effective resolution of users issues/queries.Empowering development team to focus & build new features.Drive continuous improvement & provide key health indicators for the products.Ensuring smooth product operations.Technical Experience:Minimum of 4 to 7 years of experience working in supporting complex production systems. Proficient in Python scripting. Proficient in SQL programming. Basic knowledge/Interested to learn technologies like HTML, CSS, and JavaScript (Frontend related)Added advantage of having some knowledge in big data tech stack viz Hive, Impala, Sqoop, Oozie, HDFS, Hive, Kafka, etc.Involved in RCA (Root Cause Analysis) using application and system error logs. Good communication and presentation skills - constant communication, regular update, and follow[1]ups with various stake holders. Openness to share knowledge & learn together. Interested to learn new technology.Good understanding of production support process.Ability to listen to team members and communicate instructions effectively.Quick learner, self-motivated, should have ability to lead and direct team members.Should have ability to take proactive steps in managing problems. Added advantage of having some fundamental knowledge in Machine Learning.Qualifications: • Bachelor's Degree Computer Science, a related field or equivalent experience Req

Project Role: Full Stack LeadWork Experience: 8+ Years.Work location: Bangalore/Kochi/GurgaonWork Mode: HybridMust Have Skills: React Js + Node JS + Any Database (preferrable Azure database) Job Overview:Join global organization with 82000+ employees around the world, as a Lead Full Stack Developer based in IQVIA Bangalore. You will be part of IQVIAs world class technology team and will be involved in design, development, enhanced software programs or cloud applications or proprietary products.The primary duties and responsibilities of the "Full Stack Software Engineer" include, but are not limited to:-Designing, coding, and debugging software.-Improving the performance of existing software.-Maintaining and upgrading existing software.-Recommending new technologies that can help increase productivity.-Investigating software-related complaints and making necessary adjustments to ensure optimal software performance.Knowledge/Skills:8+ years of experience-Proven expertise and hands-on experience using front-end frameworks such as ReactJS, JavaScript / Typescript, and backend development with JavaScript / Typescript using NodeJs-Using cross-platform frameworks such as Spring Boot-Strong analytical skills-Good communication skills-Excellent organizational skills-Code reviews for junior developers-Experience in designing high performing systems-Proven experience applying DevOps principles and developing CI/CD using automation tools such as TerraForm-Proven experience in software development methodologies.-Proven experience building complex web systems.-Ability to multi-task.-Experience with Azure

Job Title - Associate Medical Data Review ManagerLocation - Bangalore and Thane Work Mode - Hybrid (3days WFO and 2 days WFH in a week)Education qualification - MBBS/MD is a must. PURPOSE Provide expert skills as part of a Medical Data Review team to provide efficient, quality Medical Data Review products that meet customer needs. RESPONSIBILITIES Serve as a Subject level Data reviewer (SLDR) and Identify any anomalies in patient reported data by performing Subject level Data Review that require further investigation with the clinical site to determine overall accuracy Conduct in-stream data trend analysis in support of data quality and integrity (includes protocol compliance and targeted review of patient data) Provide project management to the team in the area of Project Management and viewed as an expert in data management. Drive the delivery of end-to-end study data quality and integrity. Provide medical, clinical, and scientific advisory expertise. May act as a clinical data scientist for performing data analytics by reviewing the visualizations, identify potential issues of concern and present at multi-disciplinary team meetings and external meetings. Ensure data quality focus to audit readiness with Clinical Compliance and Systems Validation Compliance. . Define data capture requirements in line with protocol and reporting needs. Maintain strong customer relationships With guidance, track service performance and provide leadership to identify root causes of issues and implement remedial actions Ensure timely follow-up and resolution of compliance issues Serve as Subject Matter Expert (SME) Serve as POC/ Back-up POC Continuously look for opportunities to improve efficiency of tasks and quality of deliverables • Provide therapeutic area/indication training for the project clinical team. Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested. REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Good understanding of clinical/medical data. Knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology. Proven expertise in the proactive identification of issues. Demonstrated ability to plan, organize and manage resources to bring to successful completion specific study or project goals and objectives in accordance with defined quality and time based metrics. Proven ability to work within a matrix team environment requiring minimum level of supervision • Attention to detail Interpersonal and analytical skills, Must have Medical but also an operational focus towards metrics and status information to take the appropriate actions to resolve. Excellent communication, interpersonal, customer service, and teamwork skills. • Excellent organizational and problem-solving skills. Excellent project management skills and coaching skills. Ability to work with minimal supervision, using available resources, Ability to work on multiple projects and manage competing priorities Strong customer focus skills Ability to establish and maintain effective working relationships with coworkers, managers and clients.MINIMUM REQUIRED EDUCATION AND EXPERIENCE Medic with 5 year college degree or MBBS; or MD with 2+ years of clinical or non clinical experience required.. Experience in clinical data sciences at a CRO, pharmaceutical company or other medical environment with demonstrated leadership experience PHYSICAL REQUIREMENTS Extensive use of telephone and face-to-face communication requiring accurate perception of speech. Extensive use of keyboard requiring repetitive motion of fingers. Regular sitting for extended periods of time.

Project Role: Azure date engineerWork Experience: 2 to 8 YearsWork location: Be Bangalore / Gurugram / KochiWork Mode: HybridMust Have Skills: Azure Data engineer, SQL, SparkJob Overview:Responsible for the on-time completion of projects or components of large, complex projects for clients in the life sciences field. Identifies and elevates potential new business opportunities and assists in the sales process.Skills required:Experience in developing Azure components like Azure data factory, Azure data Bircks, Logic Apps, FunctionsDevelop efficient & smart data pipelines in migrating various sources on to Azure datalakeProficient in working with Delta Lake, Parquet file formatsDesigns, implements, and maintain the CI/CD pipelines, deploy, merge codesExpert in programming in SQL, Pyspark, PythonCreation of databases on Azure data lake with best data warehousing practisesBuild smart metadata databases and solutions, parameterization, configurationsDevelop Azure frameworks, develops automated systems for deployment & monitoringHands-on experience in continuous delivery and continuous integration of CI/CD pipelines, CI/CD infrastructure and process troubleshooting.Extensive experience with version control systems like Git and their use in release management, branching, merging, and integration strategiesEssential Functions:Participates or leads teams in the design, development and delivery of consulting projects or components of larger, complex projects.Reviews and analyzes client requirements or problems and assists in the development of proposals of cost effective solutions that ensure profitability and high client satisfaction.Provides direction and guidance to Analysts, Consultants, and where relevant, to Statistical Services assigned to engagement.Develops detailed documentation and specifications.Performs qualitative and/or quantitative analyses to assist in the identification of client issues and the development of client specific solutions.Designs, structures and delivers client reports and presentations that are appropriate to the characteristics or needs of the audience.May deliver some findings to clients.QualificationsBachelor's Degree ReqMaster's Degree Business Administration Pref2-8 years of related experience in consulting and/or life sciences industry Req.

Job Title: Associate Manager - Project FinanceJob Location: Thane/Bangalore Work Timing : 2:00 PM to 11:00 PMMode of Work : Office basedJob Overview:Provide project financial support and direction on complex global multi region, multi service studies, ensuring project financials are properly monitored and managed in pursuit of maximizing project profitability and cash flow. Support all project finance related activities for assigned projects in accordance with Sarbanes Oxley, Company Policy and Procedures, US Generally Accepted Accounting Principles (GAAP) and financial practices.Essential Functions:Manage staff, including professional development and performance appraisals. Review work load of direct report(s). Establish goals that will increase knowledge and skills levels by providing input on delegating tasks commensurate with skill level.Act as a financial advisor to the Project Manager, the Global Unit Head, and/or the Global Operation Head. Assist in the preparation for the Monthly Project Review, and proactively participate in meeting discussions to identify, communicate and address financial issues.Complete month-end close, providing global variance explanations to forecast.Conduct monthly review and analysis of assigned projects, including review of revenue recognition, project performance variances, unbilled/unearned and cash positions. Monitor monthly compliance reports to ensure timely reporting of revenue and billing deliverables by Project Manager.Support monthly reporting requirements for assigned projects, including unsigned contract opportunities, backlog, and other ad-hoc financial analysis as required.Review and approve work movements and changes, and final remaining revenue adjustment for assigned projects.Ensure project journal, write-offs, and financial adjustments are properly documented, reviewed and approved.Perform final configuration review and approval of the Projects and Contracts modules for assigned projects.Reconcile and monitor Unbilled, Write-off activity, Over the Limit and Contract Activation exception reports and resolve unusual activity.Monitor project and customer activity against contract terms to ensure foreign exchange rate variances and discounts are properly monitored and accounted for.Complete assigned Monthly and Quarterly Sarbanes Oxley reporting requirements.Coordinate customer and financial audit requirements for assigned projects.Ensure awareness of current Company policy and procedures and monitor project activity to ensure compliance.Partner with other Project Finance members to develop and implement process improvements.Train and mentor more junior staff.Will be assigned Global projects, large customers, therapeutic units and associated responsibilities in support of career progression planning initiatives.Perform other duties as assigned.Qualifications:Bachelor's Degree Req10 years accounting or project finance experience; including previous management experience Req OrEquivalent combination of education, training and experience. ReqKnowledge of revenue recognition, variance analysis, unbilled/unearned and cash flow management, and backlog forecasting.Knowledge of Peoplesoft Project.Knowledge of Microsoft Office applications.Strong analytical and numeracy skills.Ability to identify financial issues, develop and execute mitigating actions.Effective verbal and written communication skills.Strong influencing skillsManagement of othersAbility to prioritize and coordinate multiple work requirements to meet deadlines.Ability to establish and maintain effective working relationships with co-workers, managers and clients.

Job Title / Primary Skill: Big Data Developer (Lead/Associate Manager)Management Level: G150Years of Experience: 8 to 13 yearsJob Location: Bangalore (Hybrid)Must Have Skills: Big data, Spark, Scala, SQL, Hadoop Ecosystem.Educational Qualification: BE/BTech/ MTech/ MCA, Bachelor or masters degree in Computer Science, Job OverviewOverall Experience 8+ years in IT, Software Engineering or relevant discipline. Designs, develops, implements, and updates software systems in accordance with the needs of the organization.Evaluates, schedules, and resources development projects; investigates user needs; and documents, tests, and maintains computer programs. Job Description:We look for developers to have good knowledge of Scala programming skills and Knowledge of SQLTechnical Skills:Scala, Python -> Scala is often used for Hadoop-based projects, while Python and Scala are choices for Apache Spark-based projects.SQL -> Knowledge of SQL (Structured Query Language) is important for querying and manipulating data Shell Script -> Shell scripts are used for batch processing of data, it can be used for scheduling the jobs and shell scripts are often used for deploying applicationsSpark Scala -> Spark Scala allows you to write Spark applications using the Spark API in ScalaSpark SQL -> It allows to work with structured data using SQL-like queries and Data Frame APIs. We can execute SQL queries against Data Frames, enabling easy data exploration, transformation, and analysis.The typical tasks and responsibilities of a Big Data Developer include:1. Data Ingestion: Collecting and importing data from various sources, such as databases, logs, APIs into the Big Data infrastructure.2. Data Processing: Designing data pipelines to clean, transform, and prepare raw data for analysis. This often involves using technologies like Apache Hadoop, Apache Spark.3. Data Storage: Selecting appropriate data storage technologies like Hadoop Distributed File System (HDFS), HIVE, IMPALA, or cloud-based storage solutions (Snowflake, Databricks).

JOB TITLE: Project Finance AnalystJOB LOCATION: BangaloreWORK Timing: 2:00 PM to 11:00 PM(Pickup/Drop would be provided)Job Overview:Provide financial support, ensuring accurate configuration and maintenance of project financial data / activity within the Company's Project / Contract accounting and tracking system. Assist with the review and analysis of project financial activity to ensure adherence to identified internal control requirements and compliance with Company financial policies and procedures.Essential Functions Coordinate loading of global project budgets to financial management system, including collection of non IQVIA International Pricing (QIP) supported budgets. Review / reconcile loaded project budgets to ensure accuracy against contracted values. Coordinate loading of payment schedule. Review / reconcile loaded project payment schedule to ensure accuracy against contracted values and compliance to negotiated contract terms. Confirm setup of the Project and Contract header information. Coordinate configuration of Project and Contract modules, including assignment of Rate Sets / Plans to Activities, configuration of Contract Lines and establishment of Billing / Revenue Limits. Review / monitor rate exception reports and coordinate resolution of rate issues in a timely manner with the Global Project Services Group. Ensure review and completion of Project Check-off list throughout the project lifecycle (Activation, Configuration and Close-out). Monitor monthly compliance reports, to ensure timely reporting of revenue and billing deliverables by Project Manager. Complete project close-out procedures and communicate Project Status Action to the Global Project Services Support Group. Perform project level unbilled/unearned reconciliations as required. Monitor Unbilled, Write-off Activity and Over the Limit exception reports and resolve/escalate unusual activity. Assist in the preparation of invoice backup requirements, and client reconciliation requests as required. Complete assigned Monthly and Quarterly Sarbanes Oxley reporting requirements. Assist with other special project reporting and analysis as required. Perform any other duties as assigned.Qualifications Bachelor's Degree Req 5 years experience in a finance related role Req Or Equivalent combination of education, training and experience. Req Knowledge of Peoplesoft Project. Knowledge of Microsoft Office applications. Technical accounting skills. Data analysis and manipulation skills. Ability to exercise judgment within procedures and practices to determine appropriate action. Ability to prioritize and coordinate multiple work requirements to meet deadlines. Ability to establish and maintain effective working relationships with co-workers, managers and clients.

Job Title: Associate ConsultantWork Hours: General ,working hours: 12:00 PM to 9:00 PMLocation: Bangalore (Hybrid Mode of Work)Job Overview:Join global organization with 82000+ employees around the world, as an Consultant based in IQVIA Bangalore. You will be part of IQVIAs world class technology team and will be involved in design, development, enhanced software programs or cloud applications or proprietary products.We are seeking a Consultant with 3 to 7 years of experience. The ideal candidate will have Responsible for data extraction, validation, and analysis using various IQVIA databases. Ability to look at data and spot trends and/or anomalies in the data in (Italian Language).Job ResponsibilityOrganizational skills with the ability to multitask, work independently, and efficiently to meet scheduled deadlinesGood analytical capability, strong secondary research skills and excellent communication (Verbal / Written )Strong organizational skills with the ability to multitask and work independently and efficiently to meet scheduled deadlinesShare insights and observations with the stakeholders.Ability to compare data sets, merge data setsResponsible for data extraction, validation, and analysis using various IQVIA databasesAbility to look at data and spot trends and/or anomalies in the dataCreate Excel templates for data analysis and documentation (SOPs, Checklists) of projectsInteract with clients to manage new client transitions, query resolution and ad-hoc requestsAbility to work in a team and coordinate with team members in performing quality checks for the delivery of projects with tight turnaround timesQualifications & Skill3-5 Years of experienceFluent in Italian, with the ability to speak, write, and read the language.Language Qualification: Level Certification C2 from the Italian Culture Center or a degree in Italian Language from any university.Proficient in creating Excel and PowerPoint dashboards.Effective communication skills for interacting with internal stakeholdersAny bachelors/master’s degree. Pharma knowledge would be preferred.Power BI, Advance Excel, VBA4+ years’ experience in VBA. Should be able to work on automation and create VBA/excel dashboard.Good knowledge in MS Excel2+ years’ experience in Power BI. Should have Intermediate knowledgeSQL/Python – Good to haveExperience in managing project and people.Organizational skills with the ability to multitask, work independently, and efficiently to meet scheduled deadlinesGood analytical capability, strong secondary research skills and excellent communication (Verbal / Written )Strong organizational skills with the ability to multitask and work independently and efficiently to meet scheduled deadlinesShare insights and observations with the stakeholders.Ability to compare data sets, merge data setsResponsible for data extraction, validation, and analysis using various IQVIA databasesInteract with clients to manage new client transitions, query resolution and ad-hoc requestsAbility to work in a team and coordinate with team members in performing quality checks for the delivery of projects with tight turnaround times

Job Title / Primary Skill: Assoc Clin Data CoordYears of Experience: 1-2 YearsJob Location: Bangalore/ThaneMust Have Skills: Clinical data management, data management, rave, conduct, closeout, start upGood To Have Skills: Rave Job DescriptionProvide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager.Essential Functions• Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or serve in a leadership role in a specific data management task (e.g., coder, tester or database designer for technologies that don't require extensive programming expertise) with guidance.• May serve in the role of back-up to a DOC or DTL.• May conduct data review.• May write and resolve data clarifications.• May lead database audit team.• May develop and test databases and edit specifications.• May perform testing of programming.• May perform clinical data coding. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team." Professional Attributes Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Educational Qualification: Bachelor's Degree Clinical, biological or mathematical sciences, or related field Req • Equivalent combination of education, training and experience in lieu of degree.

Job Title / Primary Skill: Manager Clin Data MgmtYears of Experience: 12-16 YearsJob Location: Kochi/Kolkata/BangaloreMust Have Skills: Clinical data management, data management, rave, Line managementGood To Have Skills: Rave Job Description Manage and support team of Data Management professionals to efficiently produce databases that meet customer requirements.Essential Functions• Provide expert review and guidance for production of Data Management deliverables including CRF/e-CRF, database design and set-up, validation definition and programming, Data Management Plan and database deliverables to internal and external customers. Provide technical advice and solutions with internal and external customers to solve problems and improve efficiency. Ensure that staff is trained and compliant with current operating procedures and work instructions and project scope of work. Identify and address professional development/training needs of staff. Mentor staff members to develop Data Management process, system, and drug development expertise. Provide operational input into proposals and scope of work. Participate in proposal defenses.• Hold at least bi-monthly meetings with direct reports to discuss, at a minimum: project status, including timelines, delivery updates, financial aspects of the group or project, and potential risks, associated mitigation and support required; status of any initiatives that they may be involved in; the team's utilization rates; the direct report's training and other administrative obligations, such as Standard Operating Procedures (SOPs) and corporate training mandates; personnel issues; and career or training objectives.• Develop and implement plans for measuring and improving employee engagement, ensuring global consistency.• Collaborate with project leads to address work scheduling for current and projected projects, staffing needs, technological needs, and projected peak workloads, ensuring global consistency, where possible. Develop and manage associated action plans to hold members accountable.• Efficiently conveying messages from leadership to direct reports and teams, as well as effectively communicating issues and opportunities up to leadership.• Might be needed to serve as the designated substitute or alternatively ensure coverage is in place for direct reports during their absence or in case of turnover.• Attend and participate in Bid Defenses, Kick off Meetings (KOM), as applicable. Support Request for Information (RFI), Request for Pricing (RFP), and budgets, as requested.• Participate / Support internal and external audits and inspections, as required. Also ensure required staff is assigned, trained and prepared to support. Professional Attributes Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Educational Qualification: Bachelor's Degree Clinical, biological or mathematical sciences, or related field Req • Equivalent combination of education, training and experience in lieu of degree.

Job Title / Primary Skill: .NET Full stack DevelopmentManagement Level: G140Years of Experience: 5 to 8 yearsJob Location: Bangalore (Hybrid)Educational Qualification: BE/BTech/ MTech/ MCA (Minimum bachelor's degree)Primary Skills: C#. Net, SQL Server, React.jsJob Description Summary"Overall Experience: • Minimum 5+ years of experience developing enterprise scale web-based software systems using Microsoft technologies (Asp. Net MVC, C#, SQL Server, React.js etc.) • Experience of working in a global environment for development projects and leading teams • Experience in Agile development practices, ideally working as part of a Scrum team • Ability and willingness to learn new programming languages and techniques across the full stack (UI, middle tier, database, infrastructure) • Good knowledge of software development best practise e.g. TDD, BDD, Continuous Integration, Continuous deployment Technical: • Hands on experience in ASP.NET, C#, SQL Server, React.js , MVC, Entity Framework • Hands on experience writing SQL queries, Stored procedures, functions in SQL Server • Hands on experience writing unit tests (NUnit, Junit etc) • Experience in front end development using Javascript, jQuery and modern frameworks such as React: • Experience with software configuration management tools (e.g. TFS, Git, Jenkins, TeamCity) • Experience with search solutions, ideally Solr • Experience using techniques to communicate and describe architecture and design e.g. UML, ER, Process Diagrams, Block Diagrams Soft Skills: • Good communication, interpersonal and problem-solving skills • Good team player Expected: • Be the technical expert for the platform, understanding all aspects including Asp.Net MVC, JQuery, C#, Sql Server • Interpret requirements then recommended and communicate the technical solution. • Participate in feature development as part of a Scrum team including estimating, implementation across the full stack, writing unit tests, writing acceptance tests • Work closely with BA, ETL/DB and QA team on the assigned modules • Review and get the design approved from the leads and onshore stakeholders • Ensure high quality code to QA team Other contribution: • Participate in organization activities"

Project Role: ConsultantWork Experience: 6 to 10 YearsWork location: Bengaluru/Gurgaon.Work Mode: HybridJob Overview Provides high quality, timely development, and on-time input to client solutions for the pharmaceutical and related industries. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions to leading small teams. Essential Functions Leverages business experience and acumen in identifying strategic alternatives and project approach to client questions. Conducts primary and secondary research and analyzes research to identify key findings and learnings. Creates sections of reports, presentations, workshops, and other client deliverables, under general guidance from experienced team leaders. Communicates findings and recommendations. Assists with business development and proposals. Works independently or as part of a team, with some responsibility for managing and developing the career and skills of staff. Performs quantitative or qualitative analysis to assist in the identification of client issues and the development of client deliverables. Develops broad knowledge of related consulting methodologies and pharmaceutical market through the delivery of consulting engagements and participation in formal and informal learning opportunities. • Serves as the day-to-day manager for projects and working closely with clients. Leads some learning, development and recruiting programs. Qualifications Master's Degree. 7 or more years relevant experience. Prior experience or avid interest in the healthcare and life science industries. Project management experience. Adaptability and an ability to learn quickly and apply new knowledge. A willingness and ability to travel

Role: Centralized Monitoring AssistantSkill: Must have Good Clinical Practices (GCP)Mode: Hybrid (3 Days Work from Kochi office & 2 days from HOME)Experience: 0.6 Month to max 3 years of Exp Only.Job Location: Kochi and Ahmedabad Educational Qualification: Graduate/Post Graduate in Life SciencesPURPOSE• Engage in company training program to gain knowledge and skills required to provideadministrative support to• projects in accordance with SOPs, policies, good clinical practices, and applicable regulatoryrequirements.• Meeting quality and timeline metrics under direction of line manager and/or other designatedteam membersRESPONSIBILITIES Complete appropriate role-specific training to perform job duties. Under supervision, perform assigned administrative tasks to support team members withproject execution• (examples of such tasks include but not limited to running system reports, preparing anddistributing status• reports, creating and maintaining study documents, etc.). Under supervision, assist in updating and maintaining systems within project timelines/plans. Perform the activities as per the task list delegated by Centralized MonitoringSpecialist/Centralized Monitoring Lead.REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Basic knowledge of applicable research and regulatory requirements, i.e., ICH GCP andrelevant local laws, regulations, and guidelines. Exposure to MS Applications including but not limited to Microsoft Word, Excel andPowerPoint. Effective written and verbal communication skills including good command of Englishlanguage. Effective time management skills. Results and detail-oriented approach to work delivery and output. Ability to establish and maintain effective working relationships with coworkers, managersand clients Strong listening and phone skills. Good data entry skills.

Automation Developer Responsibilities• Reviewing software requirements and preparing test scenarios.• Collaborate with QA Engineers to develop effective strategies, create test plans and test cases • Develop automation scripts and execute both Automated and manual test cases and test Scripts• Analyzing test results on database impacts, errors or bugs, and usability.• Help troubleshoot issues• Work with cross-functional teams to ensure quality throughout the software development lifecycleQualifications• Bachelor's or equivalent experience• Test automation: 5 years • 6-8 work experience.• Data Testing 3+ years.• Experience testing in an Azure environment.RequirementsTechnology - Java jdk 11, Eclipse , Junit 5 ,Maven ,Selenium ,Spring framework GIT code repo ,Sl4j , Azure Pipeline • Familiarity with medical claims segments and transactions • Nice to have experience with Healthcare Insurance Industry• Up-to-date knowledge of software test design and testing methodologies.• Familiarity with Agile frameworks • Ability to write come up with test strategy and write test cases • Ability to document and troubleshoot errors• Working knowledge of test management software• Industry experience with a Healthcare Insurance company.• Experience in developing and maintaining automated tests a plus• Experience testing both Web and Mobile applications• Excellent communication and critical thinking skills.• Good organizational skills and detail-oriented mindset• Analytical mind and problem-solving aptitude

Job OverviewProvide project related assistance to assigned project teams.; Ensure all work is conducted in accordance with standard operating procedures, policies, good clinical practices and applicable regulatory requirements.; Meeting quality and timeline metrics.;Essential Functions• Complete appropriate role-specific training to perform job duties.;• Under supervision, provides study level administrative support to the clinical study management team (examples of such tasks include, but not limited to running system reports, preparing and distributing status reports, creating and maintaining study trackers, follow-up for outstanding issues, etc.).;• Under supervision, assist in updating and maintaining systems within project timelines/plans and driving tracking compliance in various systems to enable credible data for analysis.;• Perform the activities as per the task list delegated by CMS leads.;• Assist CMs in the preparation of i-site pack for their respective sites and countries for assigned studies, by pulling associated reports.;• Perform assigned access management related administrative tasks to support team members with project execution, example of tasks includes, but not limited to processing access requests, following up with relevant vendors, etc.;• Provide support to technical solution specialist (TSS) on formulations in Excel and on the front-end part.;• Periodic review of site level KRIs and historic site performance according to Central Monitoring Plan• Facilitating early identification of site-level risk/issue(s) occurring during study conduct and responsible for identification of risk• Monitor site performance and make recommendations for timely corrective actions (eg Site Telephone Contact or Triggered Onsite Monitoring Visit)• Review the effectiveness of the recommended actions and take appropriate additional actions if no effect is observed• Review of the Study Central Monitoring Plan• Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested• Adhere to the key activities outlined in the SOW as per customer requirementsQualifications• Other Graduate/Post Graduate in Life Sciences or educational equivalent.• Requires minumum of 2 years of work experience with minimum 6 months relevant experience.• r equivalent combination of education, training and experience. Experience level may vary based on customer specific requirements.• Basic knowledge of applicable research and regulatory requirements, i.e. International Conference on Harmonisation - Good Clinical Practice and relevant local laws, regulations, and guidelines.• Exposure to Microsoft Applications including but not limited to Microsoft Word, Excel and PowerPoint.• Effective written and verbal communication skills including good command of English language.• Effective time management skills.• Results and detail-oriented approach to work delivery and output.• Ability to establish and maintain effective working relationships with coworkers, managers and clients.• Strong listening and phone skills.• Good data entry skills

Minimum 6+ Years of experience .Proven strong track record as a senior member as well as in his/her current role.sound knowledge of Python Programming and Data Management procedures.Good understanding of medical, clinical research, and Lab Data Management process and terminology.Knowledge on elicitation of the data requirements and authoring specifications. Strong customer-focus perspective with skill to guide customer communications and customer management.

JD Execute deliverables for Standardized External Data Streams. Assess external data collection requirements per protocol and planning of external data stream set-up activities and related deliverables to meet study start-up timelines. Liaise with key data stakeholders to establish the purpose of data collection and requirements for the transfer, ingestion, and structure of data for each data stream in compliance with applicable data protection laws and regulations, utilizing available standards and templates Create change requests for the definition of new test concepts or data structures relating to external data. Develop trial-specific Data Transfer Agreements (tsDTAs) accurately documenting study requirements and methods for the data transfer, ingestion, and structure. Ensure data transfer frequencies are sufficient for the agreed requirements (medical data review, central monitoring, and reporting and analysis). Liaise with external data providers to ensure alignment and agreement of tsDTA. Translate medical and scientific concepts into data mapping guidance, per agreed data model and documented in the annotated Data Transfer Agreement for use by Clinical programmers. UAT of test data transfers ensure accuracy and consistency with data specifications defined in Data Transfer Agreements. Implement data transfer mechanisms for external data streams (into CDR) including access for external data providers. Monitor availability and accuracy of external data streams, liaise with external data providers to resolve data transfer issues relating to conformance of data Education and Experience Requirements/Qualifications: Base Level: Bachelors degree or equivalent, preferably in Computer Science. Minimum of 5 years experience managing data in support of clinical research. Experience working with external data e.g., Safety Lab, PK, Simple Biomarkers, ECG, or similar. Experience working on clinical trials. Experience working in highly diverse teams within clinical research; cross-functional, global

Project Role: Lead Full stack DeveloperWork Experience: 8+ Years.Work location: Bengaluru/KochiWork Mode: HybridMust Have Skills: Angular 13 and above, NGRX, C#, RxjsJob Overview:Mandatory:Solid frontend development experience with Angular and API development experience with C#. Requires a basic understanding of common design patterns used in each.Candidate needs to have experience in a 'formal agile environment' and 1st hand knowledge of agile ceremonies.Proficient in NGRXExperienced in developing applications in a single page (SPAs) using various JavaScript frameworks like Angular.Creating reusable components, custom directives, decorators, and services to interface with both restful and legacy network services including DOM applications.Front End/UI, Healthcare and Azure Apps are mandatory.Front end technologies like HTML, JS, CSS, TS, Angular, Ionic, Material UI, Bootstrap and various other frameworks and librariesExpertise in developing in the User Interfaces and web pages using technologies like HTML 5, CSS 3 (SASS), JavaScript, NGRX, TypescriptWorked with Azure DevOps, Gitlab, along with the CI tool Jenkins.Preferable:Experience with Azure DevOps pipelines.C# Function apps in AzureNice to have but not really a showstopper:CI/CD pipelinesCosmos DB (or other NoSQL experience)Azure API ManagementCognitive search (or other search service experience)Azure Storage (or other blob storage experience)Educational Qualification:Bachelor's Degree

Job Title: Senior Medical Safety Advisor Education Qualification: MBBS/MD.Work Location: Anywhere in India.Work Mode: Home Based.Years of exp: 3yrs Clinical and 2+ yrs of PV (Exp in Oncology is a must)Pls note MCI reg is mandatory for all the foreign medical graduates. Job Overview Provide medical expertise on pharmacovigilance services to divisions as requested. The Associate Medical Safety Director participates in all aspects of Medical Safety's involvement on assigned trials and standalone safety projects with appropriate oversight from management or more senior medical safety directors. Essential Functions Perform medical review and clarification of trial-related Adverse Events (AEs) and post-marketing adverse drug reactions (ADRs) including narrative content, queries, coding, expectedness, seriousness, causality and company summary Compose, edit and medically review Analyses of Similar Events (AOSE) for expedited cases as appropriate based on regulatory requirements Serve as an internal consultant to pharmacovigilance case processing teams on projects being supported Provide aggregate reviews of safety information, including clinical data, to maintain oversight of a products safety profile Provide coding review of AEs, Past medical history, Concomitant medications or other medical data listings to verify and medically vet clinical data Represent safety and clinical data review findings during client meetings Provide medical review and edits to IND Annual Reports, EU Periodic Benefit Risk Evaluation Reports, EU Periodic Safety Update Reports, EU Development Safety Update Reports, US Periodic Reports Provide medical review and edits of Development Risk Management Plans, EU Risk Management Plans or US Risk Evaluation and Mitigation Strategies Provide medical oversight for label development, review and change Provide medical support and attendance at Data Safety Monitoring Board Meetings • Attends and contributes medical safety evaluation on Safety Monitoring Committees Provide medical safety contributions to the Integrated Safety Summary or Common Technical Document Provide medical review and edits to Drug Safety Reports or other benefit-risk assessments Review and sign off on both the Project Safety Plan and the Medical Monitoring Plan per medical safety scope agreed in contract Perform Medical Safety review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs) for appropriate safety content and data capture. Act as Global Safety Physician or Assistant or Back-up on projects as assigned Attend project meetings, medical safety team meetings, and client meetings as requested Ensure coverages for all medical safety deliverables within regulatory or contracted timelines Provide medical escalation support for medical information projects Provide medical escalation support for EU Qualified Persons for Pharmacovigilance projects • 24-hour medical support as required on assigned projects Maintain awareness of medical-safety-regulatory industry developments Qualifications Required MBBS/MD graduates from an accredited and internationally recognized medical school with a curriculum relevant to general medical education. Three (3) years of clinical practice experience with 2+ additional years in the pharmaceutical or associated industry in any role is required. Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research including knowledge of regulations and guidelines pertaining to safety and good clinical practice. Knowledge of clinical trials and pharmaceutical research process. Ability to establish and meet priorities, deadlines, and objectives. Skills in providing consultation and advice on multiple assignments required, as well as initiative and flexibility. Ability to establish and maintain effective working relationships with coworkers, managers and clients. A valid medical license, or equivalent, from the country or region in which he/she resides and works Preferred.

Interested candidates may share their resume at heena.gill@iqvia.comJob Description :Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures; Perform programming validation to ensure quality of analysis datasets and programming outputs• Provides programming support for project teams, including development of programming strategies, standards, specifications and programmed analysis• Support the electronic submission preparation and review• Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements; Assesses impact on programming activities• Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers• Provides leadership for ensuring quality of Global Biometric and Data Sciences (GBDS) deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices• Identifies opportunities for increased efficiency and consistency within GBDS and our interactions with strategic vendors• Independently leads and / or performs programming assignments with minimal supervision• Support improvement initiatives

Job OverviewProvide experienced technical expertise to develop process methodology for department to meet internal and external clients needs. Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements.Essential Functions• Perform, plan and co-ordinate the following for complex studies: (i) the programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing summaries and (ii) the programming of analysis databases (derived datasets) and transfers of data for internal and external clients. May perform and plan the programming of database quality control checks.• Program and plan the integration of databases from multiple studies or sources.• Develop and co-ordinate programming documentation including plans and specifications, as appropriate, for complex studies.• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to teams and department, for complex studies.• Perform, plan and co-ordinate the development, implementation and validation of new process technologies, macros and applications.• Fulfill project responsibilities at the level of statstical team lead for single complex studies or group of studies.• Understand the Scope of Work, budget and quote assumptions, estimate the work completed, manage Out of Scope and resource forecasts for single studies. May manage project budget and resource requirements, and provide revenue forecasts for single studies.• Provide training and guidance to lower level staff.Qualifications• Master's Degree Computer science or related field • Knowledge of statistics, programming and/or clinical drug development process• Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language• Good organizational, interpersonal, leadership and communication skills• Ability to effectively manage multiple tasks and projects• Excellent accuracy and attention to detail• Ability to establish and maintain effective working relationships with coworkers, managers and clients

Kindly share your updated resume to heena.gill@qvia.comRole & responsibilities Minimum 6+ Years of experience .Works collaboratively with clinical bioinformatics, biomarker scientists and study statistical programming team, to meet biomarker analysis deliverables and timelinesHas knowledge of clinical trial study design and biomarker assay types, including but not limited to Immunohistochemistry, cell phenotype, next gene sequencing.Demonstrate knowledge of CDISC standards for SDTM, ADaM and submission experience to regulatory agencies. Demonstrates SAS programming proficiency, including in depth understanding of graphical template languages and using internalmacros or writes SAS macros to automate study deliverables.Demonstrates R programming proficiency in using data science library packages including but not limited to tidyverse, pharmaverse and shiny.Demonstrate statistical knowledge, interpret complex dataset and modeling methods in both SAS and R languages.Must be familiar with Microsoft Excel, Microsoft Word, Adobe PDF. Role & responsibilities

Job Title / Primary Skill: Clinical data specialistYears of Experience: 2-5 YearsJob Location: Kochi/KolkataMust Have Skills: Clinical data management, data management, rave, conduct, closeout, start upGood To Have Skills: Rave Job Description Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. Undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager.Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or serve in a leadership role in a specific data management task (e.g., coder, tester or database designer for technologies that don't require extensive programming expertise) with guidance. Serve in the role of back-up to a DOC or DTL. Conduct data review. Write and resolve data clarifications. Lead database audit team. Develop and test databases and edit specifications. Perform testing of programming. Perform clinical data coding. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team. Professional Attributes Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Excellent organizational, communication, leadership and computer skills. Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients. Educational Qualification: Bachelor's Degree Clinical, biological or mathematical sciences, or related field Req • Equivalent combination of education, training and experience in lieu of degree.

Project Role: DWH Technical Project ManagerWork Experience: 9 to 15 YearsWork location: Bengaluru/KochiWork Mode: HybridMust Have Skills: Technical DWH Project Manager, DWH Projects, Snowflake, ETL, SQL/PLSQL , Any Data Background, Power BI Dashboards Job Description: • 10+ years of relevant experience in the Databases like Oracle, SQL Server, Netezza, DB2 • Experience managing projects as a Technical project manager or Scrum Master • Strong hands-on in ETL and Data warehousing projects involving large enterprise datasets • Experience managing BI projects using tools like Power BI, Tableau, Qlik etc. • Strong data analysis, querying and reporting hands-on. • Ability to write complex queries to build complex datasets is a must • Working knowledge of Snowflakes is mandatory. Alternatively, a strong hands-on with Hadoop, Spark and Hive is equally valid • Hands-on with any of the orchestration tools is a must. Airflow knowledge is a definite plus • Experience working on any of the cloud platforms is a definite plus. • Strong hands-on with healthcare data is a definite plus • Should have led a new client configuration of a product / platform from the scratch and handled it till BAU • Strong working experience in Agile projects • Good exposure to CI/CD, Jenkins and DevOps ways of deployments is a must. • Proactively identify and address the client specific issues and address them. • Liaise technically with the core product team and explore areas of platform customizations, performance optimizations • Ability to lead a client specific delivery team to handle the technical requirements as part of the delivery/offering team • Strong communication and ability to lead multiple client deliveries/offerings in parallel • Validates the project scope, plans and schedules for moderately complex projects; adheres to metrics for project success and begins to suggest appropriate metrics; provides input to and applies standards (e.g. delivery process, roles and responsibilities, operational norms, compliance). • Identifies risks to program success and escalates to management as necessary. • Manages project delivery process, scope, and costs of moderately complex projects under broad supervision; drives completion of the project. • Manages stakeholder relationships; develops and executes communication plan. • Manages change by identifying impacts of the project, building awareness and support for change within the organization, and contributing to development of training. • Evaluates project results against success metrics; recommends or implements changes to processes, resources and solutions that improve productivity and end product. • Consistently delivers established team reporting and guidance metrics.Qualifications • Bachelor's Degree Computer Science, a related field, or equivalent experience • 10+ years of experience in software and/or product development • Project management education and experience.

Job Overview Provide comprehensive clinical lab data expertise as part of a team to develop and maintain Laboratory Data Management (LDM) tasks for the studies awarded to IQVIA Laboratories and meets the external client data reporting needs. May be required to support the development of new systems and processes related to the electronic data transfer process, or the configuration of business rules and master data in study and laboratory information systems. Understand and comply with core standard operating procedures and working instructions. Essential Functions • Capable of taking up, independently or providing inputs for, Python programming activities pertaining to ongoing study requirements or any other adhoc projects in the department • Create and/or review all appropriate data management documents • Understand and comply with core standard operating procedures and working instructions • Develop and maintain good communications and working relationships with LDM team. Serve as back-up for other Data Team Leads • Interact with internal and external team members to negotiate timelines and responsibilities • Train and mentor junior staff in DM expertise • Ensure service and quality meet agreed upon timelines and deliverables in data transmission agreements. Ensure quality checks performed on data files before transmission and obtain peer-review where required. Review own work for accuracy and completeness • Record all evidence of the data transmission process from data file definition to closure of study • Ensure that all specification and design documentation are filed and stored according to company policy • Ensure the internal and external customer queries are timely addressed and resolved effectively • Multiple communication styles and skill to effectively broker, audience specific [peers, senior team members, internal/external customers] business and interpersonal relationships that lead to positive outcomes and successful business results • Perform other duties as directed by the functional manager • Manages the delivery of projects through full data management study life-cycle, from setup to lock • Supports the identification and resolution of service level issues, as well as the proactive development of contingency plans to mitigate laboratory risk • Works with customers, scientific team, data managers and internal team members to manage issue escalation, workload projections, and provide technical expertise • Interacts and communicates with internal and external customers to ensure that timelines are met and that data is delivered following company guidelines and regulatory compliance • With guidance, manages project timelines and quality issues, and identifies and justifies out-of-scope client requests • Assists internal team with data entry, review and validation of laboratory reports, and serves as back-up contact when needed • Performs comprehensive quality control and edit check procedures • Supports service delivery with comprehensive process and technical expertise in executing projects which includes identifying and resolving issues. Effectively works on corrective and develop preventive action plans Qualifications Bachelor's Degree (B. E, B. Tech, B. Pharm): Computer Science with Software Configuration and Validation experience Req • 2-3 years of experience in Data Management and Python Programming. .

Job Title / Primary Skill: Big Data DeveloperYears of Experience: 2 to 8 yearsJob Location: Kochi (Hybrid)Must Have Skills: BDF with Hadoop, Spark, Scala, and SQLEducational Qualification: BE/BTech/ MTech/ MCAExperience: • Minimum 2+ years of experience in Big Data development. • Good understanding of SDLC. • Experience with Agile or iterative development methodologies is a plus. • Prior experience in Healthcare Analytics domain is a plus. Technical: • Minimum 2+ years of hands-on experience in Big Data. Fluent in big data engineering development using the Hadoop/Spark ecosystem. • Experience with SQL, Scala, Spark, Python.Experience working in the Hadoop ecosystem (impala, Hive, UDF, Etc) • Data ingestion and integration into the Data Lake using the Hadoop ecosystem tools such as Sqoop, Spark, Impala, Hive, Oozie, Airflow etc. • Candidates should be fluent in the Python / Scala language Professional Attributes: Should have good communication skill. Team player willing to collaborate throughout all phases of development, testing and deployment. Ability to solve problems and meet the deadlines within minimal supervision.

Greetings from IQVIA!We are looking for Consultant/Associate Consultant, Primary market research for Bangalore/Gurugram/Pune locations. Please apply using below link and embark on an extraordinary professional journey. https://jobs.iqvia.com/en/job/bengaluru/primary-market-research-consultant-associate-consultant/24443/76903943984?utm_source=social&utm_medium=recruiter&utm_campaign=ajay-nvProject Role: Primary Market ResearchWork Experience: 2 to 8 YearsWork location: Bengaluru/GurgaonWork Mode: HybridMust Have Skills: Primary market research, Quantitative/Qualitative research, Pharma/Lifescience domain experienceAbout the teamThe role is within the Research & Intelligence Team (R&I), whose aim is to deliver market research solutions, comprising mainly of PMR (Primary Market Research) to generate relevant insights for clients.Responsibilities:Deliver in depth, comprehensive PMR reports and support ad hoc PMR projects in the multiple therapy areas like immunology, respiratory, rare diseases, neurology, diabetes, oncology etc. (non-exhaustive)Analyze primary data collected through interviews/surveys and create PowerPoint reports to provide information on different client objectives and requirementsDemonstrate excellence as an individual contributor with minimal support from peers/team lead, together with the ability to work independently with onshore team members, driving high productivity/ efficiency, and creating appropriate performance reviews and capability development planShould have flair to work across different sectors within HealthCare industry (Pharmaceutical, Life Sciences, Biotechnology and Healthcare services)Quality control, overview and to ensure deliverables are client ready. Should be able to manage client and stakeholder communication - via emails and conference callsProject types: Primary market Research (Qualitative and quantitative)- Patient Journey, brand performance trackers (involving multiple indications), market understanding, pricing etc.What were looking for:Relevant Experience of 2+years . Preferential consideration will be given to candidates with experience in carrying out consulting and market research projects in the pharmaceutical areaExperience/ academic background for sectors encompassing HealthCare industry (Pharmaceutical, Life Sciences, Biotechnology and Healthcare services)Experienced with qualitative and quantitative PMR research and on a variety of therapy areas as listed aboveHigh skills of interpretation and analysis (quantitative, qualitative and integration of different sources of data assets) - This would include thinking through the client business issue, adding the right context to the request (therapy area, business issue etc.) and developing a tailored, innovative solution to address the clients business objectivesAbility to understand the link between client needs, data and its applicationExperience in designing/ developing questionnaire and discussion guide as per clients objectiveExcellent interpersonal, oral and written communication skillsGood innovative thinking abilities and solution-oriented approach to workShould be very comfortable with MS Word, PowerPoint, and ExcelEducational Qualification:Bachelor's Degree Life Sciences / Economics / Business Pref OrMaster's Degree Life Sciences / Economics / Business Pref Or

Interested candidates may share their resume at heena.gill@iqvia.comJob Description :Create SAS programs to generate derived analysis datasets and content for tables, listings, and figures; Perform programming validation to ensure quality of analysis datasets and programming outputs• Provides programming support for project teams, including development of programming strategies, standards, specifications and programmed analysis• Support the electronic submission preparation and review• Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements; Assesses impact on programming activities• Interacts with vendors regarding project standards, programming conventions, programming specifications and file transfers• Provides leadership for ensuring quality of Global Biometric and Data Sciences (GBDS) deliverables by consistently applying standards and complying with regulatory requirements, guidance and corporate and departmental SOPs and work practices• Identifies opportunities for increased efficiency and consistency within GBDS and our interactions with strategic vendors• Independently leads and / or performs programming assignments with minimal supervision• Support improvement initiatives

Job DescriptionDevelop fit for purpose AIML models/algorithms/processes to address pharma/healthcare applications and innovative products upon completion of prototypes followed by the building of production grade algorithms/automation engines for client deliverables. Test for viability in order to deliver final products to clients. Able to bring newly researched ideas to reality quickly and on a large scale. Design, build, test, and deliver products from post-prototype to client delivery.Essential FunctionsAssists with the ongoing development and implementation of an enterprise architecture.May devise and present business cases and program release plans to senior management with priority recommendations to maintain and evolve this architecture. Builds effective business relationships with business line managers and provides technical and system expertise as input to product concepts.May assist product development management to define IT strategic direction and assists in the mapping of projects to that strategic direction whilst ensuring product capabilities and process improvements are delivered over time within the framework of the IQVIA enterprise architecture.Participates in cross-functional product development teams, may also act as a consultant to provide system and technical advice.Keeps up to date with technology changes and identifies opportunities for implementation in future systems.Participates in R&D projects and may run those projects in compliance with standard project management practices.May mentor and assist lower level architects and business analystsQualifications10+ years of experience in engineering roles with team management experience 5-7 relevant years experience on NLP, Machine Learning and Deep learning5-7 relevant years of experience on Python Extensively work on NLP applications, ability to work on Machine learning model, Deep learning developmentKnowledge of LLMs, fine tuning and deploymentExperience annotated datasets for Supervised Learning methods and correctionExperience on text to transform natural language into useful featuresFind and implement the right algorithms and tools for NLP tasksPerform statistical analysis of results and refine modelsExtend ML libraries and frameworks to apply in NLP tasksExperience on ORM, SQL Alchemy, Alembic is a mustExperience on Writing on effective and scalable codeExperience on Unit Testing using Pytest or equivalent framework A deep understanding and multi-process architecture and the threading limitations of Python.Familiarity with server-side templating languages including Jinja 2 and Mako is good to haveExperience on REST API, Flask API, Fast API is must, Django or Pyramid framework is good to haveKnowledge of NER, Knowledge graphs is good to haveEducation QualificationMaster's Degree Masters Degree in Machine Learning, Statistics, Computer Science, Physics, Math, or related field

Job Title - Safety Aggregate Report Specialist 2.Skills required - Signal detection/Signal Management.Years of exp required - 4+ yrs exp in Signal Mgt. Work location - Anywhere in India.Work Mode - Hybrid/Remote.Job Overview.Apply knowledge and expertise for Safety Aggregate Report and Analytics (SARA) Center deliverables including safety aggregate reports, literature surveillance, signal management activities and benefit risk management documents. • Serve as principal owner of the SARA deliverable and have responsibility for completion of the deliverable in compliance with all applicable service level agreements (SLA). • Lead, author and finalize aggregate reports, including but not limited to PBRERs/PSUR, DSURs, PADERs, RMPs, ACOs, and line listings • author responses to regulatory agency/ Pharmacovigilance Risk Assessment Committee (PRAC) inquiries, as required. • Conduct/Lead ongoing literature safety surveillance for marketed and investigational products. Assist with the identification of ICSRs from literature, evaluation of events of special interests as well as aggregate data review. • Act as Signal Management Lead on post-marketing and clinical trial projects. Set-up, implement, organize (including documentation) and lead safety management teams. Set-up and update products' signaling strategies. Author and/or QC review all types of signal management deliverables. Lead/ conduct ongoing signal detection activities as per agreed signaling strategies, perform signal validation and signal evaluation analyses for proactive and timely identification of signals and characterization of risks. Responsible for full documentation and tracking of signals. • In a PV support role, lead/author and/or QC review safety responses to regulatory agencies/PRAC and justification documents to support labelling documents.• Interface with clients and other functional groups within Lifecycle Safety and other business units, such as Regulatory affairs Reporting (RR), Real World Late Phase (RWLP), Medical Writing, Clinical Research, Quality, Knowledge Quality Management (KQM), Pharmacovigilance Support (PVS), Project Leads (PL), Medical Safety Advisors (MSA), Qualified Persons for Pharmacovigilance (QPPV) / Pharmacovigilance Contact at National Level (PCNL), Library Information Services (LIS), Safety Operations (SO), and Information Technology (IT), as needed. • Participate in internal and external audits and inspections, as required. • Contribute to achievement of departmental goals e.g. utilization realization and productivity metrics. • Read, acknowledge and adhere to all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented. • Serve as the interface between the global project lead and the working team • conduct regular lessons learned with the working teams to ensure all information from the customer is cascaded to the relevant team members. • Provide mentorship and training to less experienced resources. • Provide regular reports to overall project manager and department management on project metrics, SOW changes, client requests or concerns • participate in project review meetings with management • communicate and document project issues to project team members and department management in a timely manner. Ensure Good Documentation Practices (GDP). • Support and/or contribute to technology / innovation activities. investigators, medical monitors, site coordinators and designees to address project related issues. • Attend project team meetings and provide regular feedback/ inputs to Operations team manager on operational project metrics, out of scope work challenges/issues and successes. • To liaise with client in relation to details on day to day activities as needed. • Contribute to achievement of departmental goals • Perform other duties as assigned

Job Title - Safety Aggregate Reporting Manager.Skills Needed - Aggregate Reports Authoring.Years of exp required - 7+ years in AR authoring.Work Location - Anywhere in India.Work Mode - Hybrid/Home Based. Job Overview.Act as a stand-alone global functional lead at a project level applying experience, knowledge and expertise for Safety Aggregate Report and Analytics (SARA) Center deliverables including but not limited to safety aggregate reports, literature surveillance, signal management activities and benefit risk management documents. Actively contribute to Lifecycle Safety global process initiatives and work in close collaboration with the safety customer delivery management team regarding project/client initiatives. Ensure team is following standard best-in-class practices established by the SARA infrastructure. • Serve as a stand-alone global lead for aggregate reporting, signal management, or literature survellance projects. • Lead, author and finalize aggregate reports, including but not limited to PBRERs/PSURs, DSURs, PADERs, RMPs, REMS, ACOs, line listings • and author responses to regulatory agency/ Pharmacovigilance Risk Assessment Committee (PRAC) inquiries, as required. • Act as literature lead, back-up lead, reviewer/QCers to conduct ongoing literature safety surveillance for marketed and investigational products. Assist with the identification of ICSRs from literature, evaluation of events of special interests as well as aggregate data &/or signal detection relevance review. Author and/or contribute to literature deliverables for aggregate reports &/or signal management activities meeting strict regulatory timelines. • Act as Signal Management Lead on large and/or complex post-marketing and clinical trial projects. Set-up, implement, organize (including documentation) and lead safety management teams. Serve as subject matter expert across projects for complex data mining methodogies and algorithms on internal and external safety datasources. Oversee/set-up and update products' signaling strategies. Oversee/author and/or QC review all types of signal management deliverables. • Oversee/conduct ongoing signal detection activities as per agreed signaling strategies, perform signal validation and signal evaluation analyses for proactive and timely identification of signals and characterisation of risks . Accountable for full documentation and tracking of signals. At project level, maintain compliance, prepare metrics and KPI, present at audits and inspections. • In a PV support role, act as functional lead and oversee/author and/or QC review safety responses to regulatory agencies/PRAC and justification documents to support labelling documents. • Provide training to SARA staff for qualification on SARA deliverables • May perform quality check of all assigned SARA deliverables • be responsible for the quality of the final SARA deliverable to client regulatory, IQVIA regulatory reporting (RR), and regulatory authorties. • Provide consultative guidance to internal and external stakeholders in the for all SARA deliverables. • Act as mentor to and coach to project team staff and direct line reports. • Interface with clients and other functional groups within Lifecycle Safety and other business units, such as Regulatory affairs Reporting (RR), Real World Late Phase (RWLP), Medical Writing, Clinical Research, Quality, Knowledge Quality Management (KQM), Pharmacovigilance Support (PVS), Project Leads (PL), Medical Safety Advisors (MSA), Qualified Persons for Pharmacovigilance (QPPV) / Pharmacovigilance Contact at National Level (PCNL), Library Information Services (LIS), Safety Operations (SO), Business development (BD) and Proposals, and Information Technology (IT), as needed • Participate in internal and external audits, as required. Lead audit preparation activities in advance to audit and ensure audit readiness of project • Review project files and contact lists on a regular basis to ensure compliance with SOPs • Lead functional team and contribute to achievement of departmental goals e.g. utilization realization and productivity metrics. • Read and acknowledge all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented. Ensure Good Documentation Practices (GDP). • Serve as the interface between the global project lead and the working team • conduct regular lessons learnt with the working teams to ensure all information from the customer is cascaded to the relevant team members. • Provide mentorship and training to less experienced resources. • Provide regular reports to overall project manager and department management on project metrics, statement of work (SOW) changes, client requests or concerns • participate in project review meetings with management • communicate and document project issues to project team members and department management in a timely manner. • Contribute to resource needs and resource allocation based on workload to ensure appropriate compliance with report submissions. • Build a positive, collaborative team environment with SARA team members, lead by example and provide training and mentoring for local project leads and less experienced team members. • Contribute and assist in global/local working groups as applicable in implementation of new operational initiatives, identification and implementation of process efficiencies. • Participate in the review of existing standard operating procedures (SOPs). • Proactively identify issues and propose solutions. • Provide consultative guidance to internal and external stakeholders for all SARA deliverables. • Suggest, drive, and implement continuous process improvements across all SARA center services. • Collaborate with line managers to resolve project performance related issues of staff.

Job DescriptionProject role: Associate Clinical Data Coordinator/Clinical Data SpecialistWork Experience: 1-5 YearsWork Location: Kochi/Kolkata/Thane/BangaloreWork Mode: Hybrid(Office based)Must have skills: Clinical Data Management ,Rave, Medidata Rave Job Overview Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager. Essential Functions • Serve as a Data Operations Coordinator (DOC) for one protocol with less then 5 operations staff (excludes DE) or 15+ easy to moderately complex central laboratory studies, or serve in a leadership role in a specific data management task (e.g., coder, tester or database designer for technologies that don't require extensive programming expertise) with guidance. • May serve in the role of back-up to a DOC or DTL. • May conduct data review. • May write and resolve data clarifications. • May lead database audit team. • May develop and test databases and edit specifications. • May perform testing of programming. • May perform clinical data coding. Understand and comply with core operating procedures and working instructions. Meet objectives as assigned. Develop and maintain good communications and working relationships with CDM team." QualificationsBachelor's Degree Clinical, biological or mathematical sciences, or related field Req.Equivalent combination of education, training and experience in lieu of degree.Medical terminology exposure. Excellent organizational, communication, leadership and computer skills.Ability to exercise excellent attention to detail. Ability to act independently and with initiative required to resolving problems.Ability to establish and maintain effective working relationships with coworkers, managers and clients.Medical terminology exposure. Excellent organizational, communication, leadership and computer skills.Ability to exercise excellent attention to detail.Ability to act independently and with initiative required to resolving problems. Ability to establish and maintain effective working relationships with coworkers, managers and clients

Job DescriptionCandidate should have experience in Design and develop reports, gathering the requirement from functional team and deliver the reports with quality.Technical Skills 1.Node.js, 2.MongoDB 3.Jasper reporting Desired Skills 1.Communication Skills 2.Good documentation skills 3.Knowledge of GIT, JIRA 4. Knowledge of Healthcare domainJob Overview Assists with the design/development of reporting solutions requiring healthcare domain knowledge and reporting tool expertise. Troubleshoots code issues and continuously evolves IQVIA's platforms to meet user requirements/needs. To develop integration API using NodeJS and MongoDB and support the various types of Reports such as statistical, MIS, patient transational reports, etc Essential Functions • Assists with the design/development of reporting solutions requiring healthcare domain knowledge and Reporting tool expertise. • Designs and develops reports using Nodejs, MongoDB, and Jasper reporting tool • Troubleshoots code issues and continuously evolves IQVIA's platforms to meet user requirements/needs. • Reviews Technical specifications, functional specifications and other validation deliverables as assigned. • Develops a basic understanding of industry and IQVIA-specific quality standards. • Supports development projects based on specific instructions and with limited discretion. • Performs thorough testing and deliver with quality • Typically requires 3-6 years of prior relevant experience. Qualifications • Bachelor's Degree Computer Science, a related field, or equivalent experience

Job description :Project Role : Clinical Database Validation SpecialistWork Experiences : 3 to 6 Years Work location : Kochi Work mode: Hybrid Job OverviewConduct testing activities and provide comprehensive testing expertise to produce efficient, quality database that meets customer requirements. Provide support in creation of Test Plan and handling of validation projects. May act as Validation Team Lead. May undertake selected team leadership activities under supervision of Manager. Job Responsibility :Independently conduct testing activities to validate Edit Checks, other components, SAS listings,Transfer program and custom reports in platforms like Inform, RAVE, OCRDC, Oracle Clinical.Should have high expertise in Testing activities and excellent knowledge of Database.Advanced understanding of database structures.Perform eCRF and Time & Events QC as per QC checklist.Provide support to Validation Team Leads as required and contribute towards creation of testcases, documentation and communication with internal customers.Support Validation Team Lead in overall management of validation projects. May take complete responsibility for delivery of a validation project.Understand all the documentation requirements with regards to validation very well andupdate all relevant documents in a timely manner. May monitor documentation compliance for junior team members.Ensure validation processes and best practices are being followed strictly by self and team. May assist with creation/review of now processes/best practices.Communicate status of the projects to the Validation team Lead/Manager/ Data Team Lead/Programmer.Support Validation Team Lead/Manager with daily tasks allocation for validation projects.Escalate problems to the attention of the Validation team Lead or Manager.Conduct Quality Reviews of Testing projects on an ongoing basis as applicableConduct Knowledge Sharing and Lessons Learnt sessions regularly.Review and update relevant documents accurately and completely on time. May document all testing documentation in eDMSF. Qualifications :Bachelor's Degree Bachelor in Science/Computer science/Information Technology or Bachelor in Technology 2- 4 years of relevant clinical DB Testing experience in CDMS Platforms and total exp being 4+ years

Project Role: Power BI DeveloperExperience: 2-5 yearsJob Location: BangaloreWork Mode: HybridMust Have Skills: Power BI, DAX, SQLJob Responsibilities:Deliver best value and high-quality service. Build automated interactive dashboards using BI technologiesAnalyze data from multiple sources to derive questions and insightsCreate visualizations to show KPIs efficientlyUse optimal data modelling / processing techniques for improved performanceDefine requirements and provide simplified explanationsAssist the other reporting team with setting up the BI frameworkHands on working experience in Power BI, Tableau, Excel /SQL Assist in the coordination of project start-up activities, creation of global programs, tracking spreadsheets, and other required documentation. Technical Experience:Minimum 1 Years of experience in a business intelligence role (preferably in Healthcare sector)Strong development knowledge and expertise in Power BI dashboards (Knowledge of DAX queries and Power Query)Strong development knowledge and expertise in building interactive dashboards Tableau and SQLknowledge of other BI technologies such as Spotfire, Qlik sense will be a plusEducational Qualification: BTech/BCA/MTech/MCA

Job DescriptionCandidate should have experience in Design and develop reports, gathering the requirement from functional team and deliver the reports with quality.Technical Skills 1.Node.js, 2.MongoDB 3.Jasper reporting Desired Skills 1.Communication Skills 2.Good documentation skills 3.Knowledge of GIT, JIRA 4. Knowledge of Healthcare domainJob Overview Assists with the design/development of reporting solutions requiring healthcare domain knowledge and reporting tool expertise. Troubleshoots code issues and continuously evolves IQVIA's platforms to meet user requirements/needs. To develop integration API using NodeJS and MongoDB and support the various types of Reports such as statistical, MIS, patient transational reports, etc Essential Functions • Assists with the design/development of reporting solutions requiring healthcare domain knowledge and Reporting tool expertise. • Designs and develops reports using Nodejs, MongoDB, and Jasper reporting tool • Troubleshoots code issues and continuously evolves IQVIA's platforms to meet user requirements/needs. • Reviews Technical specifications, functional specifications and other validation deliverables as assigned. • Develops a basic understanding of industry and IQVIA-specific quality standards. • Supports development projects based on specific instructions and with limited discretion. • Performs thorough testing and deliver with quality • Typically requires 3-6 years of prior relevant experience. Qualifications • Bachelor's Degree Computer Science, a related field, or equivalent experience

Technical Skill Set Requirement Good in C#, ASP.NET, MVC, Web API,.Net Core, OOP Concepts, SQL, UI technologies (React, Typescript) Architects the UI design and the Database design Architects the Code design (Design Patterns) Develops the functionalities as per requirements mentioned in the Functional specifications using Dotnet & UI Framework/Library Follow good clinical practice and documentation practice as required. Source code management with Azure GitHub.Good to have the knowledge on Angular, Knockout, JavaScript & jQuery. Responsibilities Understands the requirements of internal and external stakeholders to develop the functionality as per client requirements and responsible User Requirement Specifications document as applicable. Prepares the Functional Specification document as per the user requirements. Prepares the Design Specification (UI design and Database) document for development of modules/projects. Responsible to implement the design patterns as per design document created and develop module/project as per design document and also mentor team members for any support. Reviews the code as per requirements & the coding standards and responsible to create unit test cases and execute the unit test cases. Plan and coordinate throughout the development stage with internal or external stakeholders to deploy the modules/projects designed/developed. Performs Performance Qualification test to ascertain the development is as per the client requirement and identify failures if any to roll back previous version and identify suitable solutions. Follows R&D SOPs throughout the SDLC and document the processes as per requirement of SOPs

Job Title / Primary Skill: AiML ArchitectManagement Level: G150Years of Experience: 8 to 14 yearsJob Location: Bangalore (Hybrid)Must Have Skills: AiMl, NLP, Machine Learning, Deep learning, PythonEducational Qualification: BE/BTech/ MTech/ MCA (Minimum bachelors degree)Job DescriptionDevelop fit for purpose AIML models/algorithms/processes to address pharma/healthcare applications and innovative products upon completion of prototypes followed by the building of production grade algorithms/automation engines for client deliverables. Test for viability to deliver final products to clients. Able to bring newly researched ideas to reality quickly and on a large scale. Design, build, test, and deliver products from post-prototype to client delivery.Essential FunctionsAssists with the ongoing development and implementation of an enterprise architecture. May devise and present business cases and program release plans to senior management with priority recommendations to maintain and evolve this architecture.Builds effective business relationships with business line managers and provides technical and system expertise as input to product concepts.May assist product development management to define IT strategic direction and assists in the mapping of projects to that strategic direction whilst ensuring product capabilities and process improvements are delivered over time within the framework of the IQVIA enterprise architecture.Participates in cross-functional product development teams, may also act as a consultant to provide system and technical advice.Keeps up to date with technology changes and identifies opportunities for implementation in future systems.Participates in R&D projects and may run those projects in compliance with standard project management practices.May mentor and assist lower-level architects and business analysts.Qualifications8+ years of experience in engineering roles with team management experience5-7 relevant years experience on NLP, Machine Learning and Deep learning5-7 relevant years of experience on PythonExtensively work on NLP applications, ability to work on Machine learning model, Deep learning developmentKnowledge of LLMs, fine tuning and deploymentExperience annotated datasets for Supervised Learning methods and correction.Experience on text to transform natural language into useful features.Find and implement the right algorithms and tools for NLP tasks.Perform statistical analysis of results and refine models.Extend ML libraries and frameworks to apply in NLP tasks.Experience on ORM, SQL Alchemy, Alembic is a must.Experience on Writing on effective and scalable codeExperience on Unit Testing using Pytest or equivalent framework.A deep understanding and multi-process architecture and the threading limitations of Python.Familiarity with server-side templating languages including Jinja 2 and Mako is good to have.Experience on REST API, Flask API, Fast API is must, Django or Pyramid framework is good to have.Knowledge of NER, Knowledge graphs is good to have.Education QualificationMaster's Degree masters degree in Machine Learning, Statistics, Computer Science, Physics, Math, or related field

Project Role: Acts as the Connected Devices Data Management point of contact for JS Programming-related activities managing Data Validation and Data Quality. Additionally, they ensure that data is processed and tracked in alignment with Sponsor expectations, regulatory and quality standards. Create Spotfire reports for Data analysis.Programs all coding deliverables; liaising with project stakeholders such as project and data operations teams; Automate manual tasks using Power Query and Power Automate.Work Experience: 2 to 4 years of relevant experience.Work location: Bangalore, Hyderabad, MumbaiWork Mode: HybridMust Have Skills: JavaScript, SQL, Spotfire, Power Automate, clinical data management.Job Overview: Prepare Edit check programs to validate data and transform Data; Automate manual tasks for efficiency.Job Responsibility: We are seeking a skilled Data Quality Specialist with expertise in SQL, JavaScript, and Power Query. The ideal candidate will be responsible for developing and maintaining data Quality and data integration solutions, ensuring data accuracy, and optimizing data workflows.Technical Skills:JavaScript programming, SQL, Spotfire for dashboarding, Power AutomateEducational Qualification:Bachelors degree in computer science engineering, or educational equivalence, in computer or related field

Role Name - Medical Data Reviewer.Educational qualifications - BDS/MDS.Experience level - 2+ yrs of exp.Location - Bangalore.Work Mode - Hybrid (3days WFO and 2days WFH). Overview of RoleReview structured clinical patient data output without direct access to medical charts to ensure medical plausibility and to determine adherence to protocol and overall completeness and readiness of the supplied patient information for next level of review. Essential Functions • Identify any anomalies in patient reported data that require further investigation with the clinical site to determine overall accuracy • Review investigation product dosing records to determine adherence to protocol and identify possible inaccurate / missed dosages • Review all reported Adverse Events (AEs) to ensure all supporting information is expected and/or implausible data is verified. Review all reported Concomitant Medications to ensure no medication is disallowed per protocol, supports an existing reported medical condition or is prescribed for a reported AE • Review all inclusion and exclusion criteria to ensure each patient meets minimum level of acceptance into the clinical trial • Ensure proper end-of-study (EOS) information is correctly documented to determine primary reason for the patient ending participation in the clinical trial • Review all laboratory results to ensure completeness of information supplied, adherence to protocol schedule of events and determine if reported laboratory values represent a potential safety condition not reported in the AE information for the patient • Review all patient reported medical history information to verify completeness of reported information, adherence to protocol expectations and its impact on other patient reported/observed information (e.g., laboratory results, AEs, etc.) • Review additional information, as necessary, to determine overall readiness of the patient information for next level review • Review all supplied Line Listings to determine data accuracy across patients within a specified group of data points • Review status information and data flow reports and take appropriate actions • Serve as POC/ Back-up POC • Interact with other Medical review staff to verify/clarify information and/or triage new data issues or prior identified action items • Attend Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested. Qualifications • Other Medic (BDS/BAMS/BHMS) with 5-year college degree or MBBS Required Or • Bachelor's Degree Clinical, biological, mathematical sciences, or related field, or nursing qualification, with 1 year of relevant work experience as MDR is Req • Equivalent combination of education, training and experience in lieu of degree Req • Understanding of clinical/medical data. • Background in Medical Terminology, Pharmacology, Anatomy, and Physiology • Excellent motivational, influencing and coaching skills • Ability to work on multiple projects and manage competing priorities • Strong customer focus skills • Ability to establish and maintain effective working relationships with coworkers, managers and clients.