Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Analyst Qualifications: BE/BTech/MCA Years of Experience: 3 to 5 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.In this role, you will be expected to develop clinical trial reports using SAS/ J-review / Congnos / SQL / PLSQL as per the study requirement. What are we looking for? Clinical Database Programming Clinical Data Management Oracle Procedural Language Extensions to SQL (PLSQL) Adaptable and flexible Ability to perform under pressure Problem-solving skills Agility for quick learning Ability to work well in a team SAS Clinical Structured Query Language (SQL) Roles and Responsibilities: In this role you are required to do analysis and solving of lower-complexity problems Your day to day interaction is with peers within Accenture before updating supervisors In this role you may have limited exposure with clients and/or Accenture management You will be given moderate level instruction on daily work tasks and detailed instructions on new assignments The decisions you make impact your own work and may impact the work of others You will be an individual contributor as a part of a team, with a focused scope of work Please note that this role may require you to work in rotational shifts Qualifications BE,BTech,MCA

Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Sr Analyst Qualifications: BE/BTech/MCA Years of Experience: 5 to 8 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.In this role, you will be expected to develop clinical trial reports using SAS/ J-review / Congnos / SQL / PLSQL as per the study requirement. What are we looking for? SAS Clinical Oracle Procedural Language Extensions to SQL (PLSQL) Python (Programming Language) R Programming Clinical Database Programming Adaptable and flexible Ability to perform under pressure Problem-solving skills Agility for quick learning Ability to establish strong client relationship Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualifications BE,BTech,MCA

Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Sr Analyst Qualifications: BE/BTech/MCA Years of Experience: 5 to 8 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.In this role, you will be expected to develop clinical trial reports using SAS/ J-review / Congnos / SQL / PLSQL as per the study requirement. What are we looking for? Clinical Database Programming Clinical Data Management Oracle Procedural Language Extensions to SQL (PLSQL) Adaptable and flexible Ability to perform under pressure Problem-solving skills Agility for quick learning Ability to work well in a team SAS Clinical Structured Query Language (SQL) Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualifications BE,BTech,MCA

Skill required: Clinical Data Services - Clinical Reports Management Designation: Clinical Data Svs Specialist Qualifications: BE/BTech/MCA Years of Experience: 7 to 11 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.In this role, you will be expected to develop clinical trial reports using SAS/ J-review / Congnos / SQL / PLSQL as per the study requirement. What are we looking for? SAS Clinical Oracle Procedural Language Extensions to SQL (PLSQL) Python (Programming Language) R Programming Clinical Database Programming Adaptable and flexible Ability to perform under pressure Problem-solving skills Agility for quick learning Ability to establish strong client relationship Roles and Responsibilities: In this role you are required to do analysis and solving of moderately complex problems May create new solutions, leveraging and, where needed, adapting existing methods and procedures The person would require understanding of the strategic direction set by senior management as it relates to team goals Primary upward interaction is with direct supervisor May interact with peers and/or management levels at a client and/or within Accenture Guidance would be provided when determining methods and procedures on new assignments Decisions made by you will often impact the team in which they reside Individual would manage small teams and/or work efforts (if in an individual contributor role) at a client or within Accenture Please note that this role may require you to work in rotational shifts Qualifications BE,BTech,MCA

Hi, We are hiring for Leading ITES Company for Lead Data Manager Profile. Job Description Perform day to day Clinical Data Management activities. Work and coordinate with the team to perform data management activities and deliver an error free quality database in accordance with the data management plan and regulator standards. Read and understand the study protocol and the timelines. Perform test data entry in TEST environment, data listing review, data reconciliation and query management tasks. Escalate/Action discrepancy in the clinical data as appropriate. Perform external checks to handle manual discrepancies and action the same. Ensure an error free, quality data with no open queries. Escalate any discrepancy in the clinical data to the study lead as appropriate. Timely completion of trainings Any other tasks deemed appropriate To perform medical data collection and analysis of Prostate Cancer Data using databases like HIS/ EMR (Electronic Medical Record) and Cases Rave, CDM (startup, close out, conduct) Client interaction and meetings. Bringing up new ideas and executing new plans to cope with the back-log. Training to new team members as and when required. Key Skills: a) Minimum 3 years of Experience in leading clinical studies/ Clinical Data Management b) Hands on experience of Study Conduct and Close Out is must c) Any Graduate To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Pune Search : Job Code # 96 b) For Position in Nagpur Search : Job Code # 97

Hi We are looking to hire Medical Data Reviewer for our Client. Please go through the JD and Apply. Responsibilities: Review subject/ patient level data for accuracy, to identify any anomalies, trends in patient reported data Review and provide inputs ion design of eCRF Review investigation product dosing Review all reported Adverse Events (AEs), Concomitant Medication and medical Ensure that any out of range data/ anomaly is verified Review all laboratory data on study subjects Review data in the form of visualizations and identify potential issues of concern Training new team members Qualifications: Bachelor/ Masters degree or equivalent in Life sciences/ Alternative Medicine (preferred) Eligibility: Good English communication skills Experience of handling clinical trial/ safety data - > 4 years To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Job Code # 359 b) For Position in Pune Search : Job Code # 360 c) For Position in Bangalore Search : Job Code # 361

Hi, We are hiring for leading ITES Company for Narrative Medical Writing Profile . Job Description Graduate or post graduate in Pharmacy, Nursing or life sciences. Certification in Medical writing or Diploma in clinical research would be desirable. Preferred experience for the Author role: Preferably 1 to 2 years of experience in medical writing domain. Life science graduate with 1 to 3 years of experience Responsibilities of Author: 1. As per process requirement and assigned primary responsibility, support CSR patient narratives (draft and QC) 2. Ensure that the narratives are in accordance with the client SOPs, guidelines and agreed timelines and comply with client quality standards 3. Perform Quality check of the narratives according to the project specific checklist and against the source documents such as patient listing, concomitant medication listing, CIOMS form etc. and log defect in the defect tracker after analyzing the defect category 4. Attention to detail, work under stringent timelines on a need basis, and switch between different projects, as required 5. Be responsible for the quality and timelines of the deliverables as designated/allocated in the project. 6. Proactive communication with lead narrative writers to meet the narrative writing quality and timelines 7. Complete assigned training within stipulated timelines 8. Provide timely data (study tracker, quality metrics, billing numbers/effort hours) for preparing relevant (e.g. quality, TAT, effort hours, etc.) and project status updates, as defined by the client requirements Key Skills: a) Grad or PG in Nursing, Pharmacy or Life Sciences b) 1 to 2 years of experience in medical writing To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Noida Search : Copy and Paste the link below https://outpace.in/job/narrative-medical-writing-4/

Skill required: Clinical Data Services - Clinical EDC Build Designation: Clinical Data Svs Specialist Qualifications: BSc/Master of Pharmacy Years of Experience: 7 to 11 years Language - Ability: English(International) - Expert What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.You will be expected to develop clinical study databases by building electronic case report forms and program edit checks as per specifications. Support any updates or changes to the study database (e.g. Protocol amendments) through the change control process. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Detail orientation Ability to establish strong client relationship Roles and Responsibilities: Data Review Report Programmers:Overall experience of 4+ years in Clinical review and reporting programming, business analytics and/or clinical trial setup, gained in the pharmaceutical industry, CRO or Life Science related industry preferred.Participate in the lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities along with providing quantitative analytical support. Provide understandable and actionable reports on clinical data and monitoring of clinical data for key stakeholders.Facilitate interaction with end user on creating specifications and working with programmers or performing the programming activities for successful delivery.Program reports of various complexity from documented requirements, within the clinical reporting systems using SQL, PL/SQL, SAS, and JReview etc. preferred.

We are looking for an Associate Analyst to join our Life Science and Healthcare (Infectious, Niche, and Rare Disease) team in Noida. We have great skill set in market research and assessment, analysis and insights and we would love to speak with you if you have skills in pharmaceutical market research. About You - experience, education, skills, and accomplishments Master s degree in pharmacy / life sciences / pharmaceutical management is required. Relevant experience of 0-1 years in the biopharma, healthcare or market research is required. Global experience and experience in directly working with global stakeholders is preferable. In-depth knowledge of at least one therapeutic area is preferable. Excellent attention to detail. Outstanding communication skills (written and oral) with ability to communicate clearly, concisely, and objectively in both written and spoken English Proficiency with Microsoft Office products (Word, Excel, and PowerPoint) Experience in analyzing and interpreting complex datasets It would be great if you also had . . . A flexible and collaborative approach to work Ability to interact and build relationships with co-workers Ability to multi-task, pivot between task and projects to adapt to changing priorities with focus on meeting committed deadlines What will you be doing in this role As part of the role, you will be Gathering and critically analyzing and interpreting clinical data and commercial information from a multitude of data sources, and draw conclusions to evaluate market trends, assess commercial opportunities and work on the various variables for market sizing / forecasts. Translate domain / therapeutic expertise, primary market research and secondary market research data into knowledge and insights for syndicated reports. Design primary market research surveys including questionnaires and conduct primary research via surveys and interviews with medical and health experts. Effectively communicate these insights to the appropriate audience via written reports. About the Team We are an international and diverse team of 13 analysts and managers located in the United States, India, Europe, and Canada making up the Infectious, Niche, Rare Diseases therapy team. The team culture is dynamic, creative, and supportive - excellence, integrity, and care are in our DNA. A modern culture environment combined with all the financial and stability advantages of working for a large business.

We are currently seeking a Software Trainee as part of our Technology team, the role will include responsibility for: Monitoring DocFlow for upcoming reports and assigning as appropriate to an Aggregate Data Management Specialist. Refreshing preliminary tables at DLP-45 and sends to the client PSSR authors Receiving requests for tables from client Communicating with the requestor to get clarity on Table Requests Answering questions on table generated from requestor Generating all the requested data tables Quality control and peer QC of data table Uploading tables into GDMS Informing PSSR Authors that the data tables are available in GDMS Creating aggregate case lists after the report was submitted to the agencies Learning and maintaining a working knowledge of data table generation systems and tools and how these are applied On-going liaison with PSSR Authors to ensure data table standards and deadlines for delivery are met Recording of key information (including workflow) to support delivery of metrics Adhering to the appropriate use of technical tools, through use of working practices and QC/QA regimes, such that regulatory and internal compliance is preserved Desirable Skills and Experience 0-1 years experience Knowledge in OOP concepts and design principles Excellent verbal communication Good team player Awareness of latest computer technology

Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Sr Analyst Qualifications: BSc/Master of Pharmacy Years of Experience: 5 to 8 years Language - Ability: English(International) - Expert What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.You will be expected to develop and review complex edit checks, patient profile listings, reports, preprocessing checks & map datasets for validation based on study requirements using different tools/techs such as Cognos / SAS, J-Review, or any other applicable systems. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Detail orientation Ability to establish strong client relationship Roles and Responsibilities: Data Review Report Programmers:Overall experience of 4+ years in Clinical review and reporting programming, business analytics and/or clinical trial setup, gained in the pharmaceutical industry, CRO or Life Science related industry preferred.Participate in the lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities along with providing quantitative analytical support.Provide understandable and actionable reports on clinical data and monitoring of clinical data for key stakeholders.Facilitate interaction with end user on creating specifications and working with programmers or performing the programming activities for successful delivery.Program reports of various complexity from documented requirements, within the clinical reporting systems using SQL, PL/SQL, SAS, and JReview etc. preferred.

Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Sr Analyst Qualifications: BSc/Master of Pharmacy Years of Experience: 5 to 8 years Language - Ability: English(International) - Expert What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.You will be expected to develop and review complex edit checks, patient profile listings, reports, preprocessing checks & map datasets for validation based on study requirements using different tools/techs such as Cognos / SAS, J-Review, or any other applicable systems. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Detail orientation Ability to establish strong client relationship Roles and Responsibilities: Data Review Report Programmers:Overall experience of 4+ years in Clinical review and reporting programming, business analytics and/or clinical trial setup, gained in the pharmaceutical industry, CRO or Life Science related industry preferred.Participate in the lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities along with providing quantitative analytical support.Provide understandable and actionable reports on clinical data and monitoring of clinical data for key stakeholders.Facilitate interaction with end user on creating specifications and working with programmers or performing the programming activities for successful delivery.Program reports of various complexity from documented requirements, within the clinical reporting systems using SQL, PL/SQL, SAS, and JReview etc. preferred.

JD for Software Developer (Angular) Software Developer Description: Do you have a burning desire to succeed and leave your mark as a top-class engineerAs a software developer you would code and work on challenging projects ranging from fixing bugs, enhancing software products, testing them and in some cases automating. Remember you can never be an architect if you have not done all the functions that an architect supports. As you grow in your role, you will have the opportunity to teach / mentor junior developers and aid in their career development. You can choose to be an individual contributor or a team leader / manager without affecting your trajectory. We don t have an emphasis on you knowing one coding language over another. We believe language skills can be developed. However, you must have a passion to learn and excel in whatever technology we adopt. We are more interested in raw talent than in an alphabet soup! The types of problems you will work on wide-range from understanding simple business processes to image processing to processing massive volumes of health care s financial and clinical data. Attributes Our engineers must be lifelong learners, develop others and act as role models for their colleagues, teams, and external partners. An ideal software developer would have several of the following attributes: Have a burning desire to learn to be an excellent developer. You should learn the foundations of good engineering practices (not taught in school or certificate programs), adapt them to your work within the framework of engineering principles at VHT and help improve existing processes. Have a strong desire to be an individual contributor under the guidance of a team leader with very little oversight Have the tenacity to ensure that you learn what you don t know down to the basics. Learn from all possible sources within the company. You should be comfortable with lack of clarity complemented with a desire to understand the business problems You should be willing to document your work and support other existing documentation (in code or requirements or tickets) by adding clarity, fixing errors or elaborating what is not obvious or can be misinterpreted. You should have a strong ability to solve problems and use software to solve these problems repeatedly Have willingness to learn new things in a fast paced / skunk works environment Willingness to experience your users issues and develop empathy for their challenges and work with your leaders to build a lasting solution Have an obsession to avoid and reduce any rework. Your work quality should be of the highest order. Rework causes a lot of delays in software. Develop a keen sense for automation and process improvement. You should learn to discern, ideate and implement use of technology to create process efficiencies to minimize or eliminate repetitive tasks You will learn to work on software and database design, development and tests process automation solutions to ensure accuracy and efficiency. Obsess over metrics to understand coverage, adoption and use of solutions. He / She will want to drive value in what we build rather than just explore technology Work with goals assigned to you. Learn to measure your work and see how they serve as key process indicators (KPIs) to help track progress Develop the skill and ability to deliver time bound projects without compromising quality and functionality Understand a variety of working technologies down to first principles, and a desire to add more to the list. Continuously seek and learn new technologies that improve our solution quality. Be aware that software reliability, scalability, performance and maintainability are all very important Be willing to work collaboratively with others on the team, SMEs and partners One important characteristic we look for is how eager you are to contribute to help others grow, and to make work and the environment better than how you found it. Requirements a Software Developer you are expected to take on complex problems and solve them from start to end. You will be responsible for: Responsible for understanding product requirements, identifying gaps and innovating processes to fill the gaps. Design, develop, and test Angular applications, ensuring they meet business requirements and are aligned with our technology strategy. Strong understanding of Angular fundamentals, including components, services, modules, and dependency injection. Proficiency in HTML, CSS, JavaScript, Bootstrap, Typescript and Angular Material UI. Experience with RESTful APIs, RxJS, NgRx (or other state management libraries). Develop reusable UI components, services, and modules using Angular best practices. Implement responsive and mobile-first design principles to ensure seamless user experiences. Write clean, maintainable, and efficient code, adhering to coding standards and guidelines. Participate in code reviews, providing constructive feedback to peers. Troubleshoot and resolve technical issues, collaborating with the QA team to ensure timely resolution. Troubleshoot complex frontend performance issues and improve load times. Optimize applications for scalability and maintainability. Stay up to date with the latest Angular versions, features, and best practices. Knowledge about cross platform frameworks like Flutter would be a plus Eager to learn new tools, technologies, and methodologies in a rapidly evolving business. We use Azure DevOps for streamlined project management and continuous integration/deployment processes. Any exposure to this will help you in our role as a software developer at VHT Constantly improving your skills, ensuring we deliver a high-quality product / platform. Turnaround bug fixes in short order and focuses on reducing rework. You will learn to work closely with product / process innovation managers, support and operations teams from time to time. If you have been working, you will have up to 3 to 5 years professional work experience as a Software Developer and demonstrated valuable contribution Familiarity with backend integration (Node.js, .NET Core, etc.) is a plus.

Software Developer Description VeeHealthtek is seeking a talented and passionate Figma UI/UX Developer to join our dynamic team. You will play a crucial role in creating intuitive and visually appealing user interfaces for our Product and Service. We are looking for someone who is not only skilled in Figma but also possesses a strong understanding of UI/UX principles and a keen eye for detail. As you grow in your role, you will have the opportunity to teach / mentor junior developers and aid in their career development. You can choose to be an individual contributor or a team leader / manager without affecting your trajectory. We don t have an emphasis on you knowing one coding language over another. We believe language skills can be developed. However, you must have a passion to learn and excel in whatever technology we adopt. We are more interested in raw talent than in an alphabet soup! The types of problems you will work on are wide-ranging from understanding simple business process to image processing to processing massive volumes of health care s financial and clinical data. Attributes Our engineers must be lifelong learners, develop others and act as role models for their colleagues, teams, and external partners. An ideal UIUX developer would have several of the following attributes: Deep understanding of Figmas features, including components, variants, auto layout, prototyping, and plugins. Ability to create and maintain complex design systems within Figma. Proficiency in using Figma for high-fidelity UI design and interactive prototyping. Knowledge of Figmas collaboration features for seamless teamwork. Experience building and maintaining design systems, ensuring consistency and scalability. Ability to create reusable components and styles. Understanding design system principles and best practices. Ability to create interactive prototypes that effectively demonstrate user flows and interactions. Knowledge of different prototyping techniques and tools within Figma. Understanding of how to use prototypes for user testing and validation. Have the tenacity to ensure that you learn what you don t know down to the basics. Learn from all possible sources within the company. You should be comfortable with lack of clarity complemented with a desire to understand the business problems Have willingness to learn new things in a fast paced / skunk works environment Willingness to experience your users issues and develop empathy for their challenges and work with your leaders to build a lasting solution Have an obsession to avoid and reduce any rework. Your work quality should be of the highest order. Rework causes a lot of delays in software. Work with goals assigned to you. Learn to measure your work and see how they serve as key process indicators (KPIs) to help track progress. Develop the skill and ability to deliver to time bound projects without compromising quality and functionality Understand a variety of working technologies down to first principles, and a desire to add more to the list. Continuously seeks and learns new technologies that improves our solution quality. Be aware that software reliability, scalability, performance and maintainability are all very important Be willing to work collaboratively with others on the team, SMEs and partners One important characteristic we look for is how eager are you to contribute to help others grow, and to make the work and the environment better than how you found it. Requirements a UIUX Figma Developer are expected to take on complex problems and solve then from start to end. You will be responsible for: Create high-fidelity UI designs and interactive prototypes using Figma, adhering to established design systems and brand guidelines. Collaborate with product managers and senior developers to understand user needs and translate them into effective design solutions. Contribute to and maintain our design system in Figma, ensuring consistency across all products and platforms. Work closely with developers, product managers, and other stakeholders to ensure seamless handoff and implementation of designs. Participate in design reviews and iterate on designs based on feedback and user testing results. Assist in conducting usability testing and analyzing results to improve user experience. Stay up-to-date with the latest UI/UX trends, tools, and best practices. Design with accessibility in mind, ensuring our products are usable by everyone. Create designs that are responsive and adapt seamlessly to different screen sizes and devices. Constantly improving your skills, ensuring we deliver a high-quality product / platform. Turnaround bug fixes in short order and focus on reducing rework. You will learn to work closely with product / process innovation managers, support and operations teams from time to time. If you have been working, you will have up to 3 to 5 years professional work experience as a UIUX Figma Developer

Mission statements The Statistical Programmer will work with Medical Affairs biostatisticians and MedHub biostatistics and programming personnel to implement statistical analysis plans and provide QC d data packages including tables, figures, and listings for use in publications (i.e. abstracts, posters, oral, presentations, and manuscripts) The Statistical Programmer will develop, implement, and document non-routine macros and advanced techniques The Statistical Programmer will ensure SOPs are followed and timelines and quality are met Collaboration Local biostatistics and programming teams Global Medical Affairs biostatisticians Global Medical Affairs Scientific Communications personnel Duties Responsibilities People Develop and maintain effective relationships and collaborations with the end stakeholders (Medical community) and local biostatistics and programming team members within the allocated Global business unit and product - with an objective to develop statistical data outputs Performance/Process Conduct appropriate post-hoc statistical analyses of clinical trial data Design, develop, test, implement, and document statistical programming in high-level software packages e.g. SAS Produce well documented data packages that include tables, listings, and figures Closely follow QC plans and timelines set by senior members of the MedHub biostatistics and programming team Remain current on advanced programming methods Customer Work closely with Global Medical Affairs biostatisticians to identify statistical analysis needs and assist in developing assigned deliverables Knowledge, Skills Competencies / Language Stakeholder management Ability to manage timelines Ability to work independently and within a team environment Advanced SAS programming skills Excellent English language knowledge - written and spoken Qualifications Bachelor or Master of Science degree or equivalent in Statistics, Computer Science, Mathematics, Engineering, Life Science, or related field Masters degree 1-2 years/B.Sc. 3-6 years of relevant experience required Requirements of the job Advanced SAS and other statistical computing software skills in a clinical data environment across multiple therapeutic areas Expertise in the use of data management applications and database/file structures, specifically with respect to CDISC requirements Autonomy in the management of activities; ability to manage multiple conflicting high priority deadlines Capacity to respond to unscheduled changes in project workload

Job Title: Medical Records & Data Management Specialist - Diagnostic Imaging Work Location : Baner, Pune Employment Type : Full-time, On-premise (8 hours/day) Department : Radiology Support / Health Information Management Position Overview As a Medical Records & Data Management Specialist , you will be responsible for handling high-volume patient records related to radiology and diagnostic imaging. You will ensure data accuracy, completeness, and timely entry into our healthcare systems. The role demands strong domain knowledge, precision, confidentiality, and a working knowledge of healthcare documentation and EMR/EHR systems. Key Responsibilities Manage end-to-end data entry and digital filing of radiology and pathology reports (CT, MRI, X-ray, Ultrasound, etc.) into the medical records systems. Cross-check diagnostic information, ensure standardization of formats, and maintain consistency in patient records. Collaborate closely with radiologists, technologists, and IT staff to ensure records are accurate and accessible. Work with PACS/RIS systems and internal EMR tools to index, tag, and archive medical documents. Track and retrieve patient data on request for follow-ups, audits, and clinical reviews. Identify missing or inconsistent data and ensure timely rectification. Maintain strict confidentiality in line with HIPAA or equivalent data privacy regulations. Support compliance for internal audits, data verification, and medical coding teams as needed. Desired Candidate Profile Education Bachelors Degree in Life Sciences, Health Information Management, Radiologic Technology, or Allied Health fields (preferred). Postgraduate diploma or certification in Medical Records Management , Health Information Systems , or Hospital Administration is a strong plus. Experience Minimum 4-6 years of experience in medical data entry, ideally in a radiology/imaging center , diagnostic lab, or hospital setup. Proven experience working with PACS/RIS/EMR/EHR platforms is essential. Familiarity with radiology report structure, medical terminology, and DICOM workflows is highly desirable. Previous exposure to HIPAA , ICD-10 , or healthcare compliance frameworks is a bonus. Skills & Competencies Strong proficiency in MS Excel and medical database tools. Strong written and verbal communication skills. Working Hours 8 hours/day, Monday to Saturday, Flexibility to work late night if required

-Contributes, with appropriate oversight, to all relevant aspects of global clinical trial(s) activities to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of the Clinical Trial Team. -Applicable to Clinical Scientific Expert IThe Clinical Scientific Expert I (CSE I) provides clinical and scientific support through all phases of a clinical study under the guidance of the (A)CD(M)D in compliance with Novartis processes, ICH GCP and regulatory requirements. This role applies the principles of clinical data review excellence and identifies clinical data insights to ensure data is scientifically plausible and to identify trends, signals and risks associated to trial endpoints and patient safety. The CSE I is a core member of the Clinical Trial Team (CTT) and may support program level activities as assigned. Job Description Major accountabilities: Implementing issue resolution plans; -Assist with program level activities (e.g., tracking of program -Managing interactions with relevant line functions including data management, drug supply management, clinical development and/or Novartis Country Pharma Organizations; -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable) Key performance indicators: Timely, efficient and quality execution of assigned trials and trial related activities within budget, and in compliance with quality standards. Proactive operational planning with effective contingency and risk mitigation plans. Applicable for Clincial Scientific Expert I: -Performing clinical data review and insights consistently and accurately which meets the Novartis quality standards, timelines, and is inspection ready. High quality contributions to study documents (e.g. protocol, ICF, clinical sections of CTA) -Clearly demonstrates Novartis Values and Behaviors (i.e. Innovation, Quality, Collaboration, Performance, Courage and Integrity. Minimum Requirements: Work Experience: Cross Cultural Experience. Operations Management and Execution. Collaborating across boundaries. Project Management. Skills: Clinical Research. Clinical Trial Protocol. Clinical Trials. Data Integrity. Learning Design. Lifesciences. Risk Monitoring. Trends Analysis. Languages : English. Skills Desired Clinical Research, Clinical Trial Protocol, Clinical Trials, Data Integrity, Learning Design, Lifesciences, Risk Monitoring, Trends Analysis

Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Analyst Qualifications: BSc/Master of Pharmacy Years of Experience: 3 to 5 years Language - Ability: English(International) - Expert What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.You will be expected to develop and review complex edit checks, patient profile listings, reports, preprocessing checks & map datasets for validation based on study requirements using different tools/techs such as Cognos / SAS, J-Review, or any other applicable systems. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Detail orientation Ability to establish strong client relationship Roles and Responsibilities: Data Review Report Programmers:Overall experience of 4+ years in Clinical review and reporting programming, business analytics and/or clinical trial setup, gained in the pharmaceutical industry, CRO or Life Science related industry preferred.Participate in the lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities along with providing quantitative analytical support.Provide understandable and actionable reports on clinical data and monitoring of clinical data for key stakeholders.Facilitate interaction with end user on creating specifications and working with programmers or performing the programming activities for successful delivery.Program reports of various complexity from documented requirements, within the clinical reporting systems using SQL, PL/SQL, SAS, and JReview etc. preferred.

Skill required: Clinical Data Services - Clinical EDC Build Designation: Clinical Data Svs Analyst Qualifications: BSc/Master of Pharmacy Years of Experience: 3 to 5 years Language - Ability: English(International) - Expert What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.You will be expected to develop clinical study databases by building electronic case report forms and program edit checks as per specifications. Support any updates or changes to the study database (e.g. Protocol amendments) through the change control process. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Detail orientation Ability to establish strong client relationship Roles and Responsibilities: Clinical Database Developers:Overall experience of 4+ years with exposure to EDC platforms like Medidata RAVE EDC, Inform, Oracle Clinical, Veeva etc. preferred.Extensive experience in database design, edit check programming, custom function programming and unit testing.Experienced in various modules such as IVRS/RWS integration and Lab administration. Medidata RAVE study builder certified preferred.

Skill required: Clinical Data Services - Clinical EDC Build Designation: Clinical Data Svs Sr Analyst Qualifications: BSc/Master of Pharmacy Years of Experience: 5 to 8 years Language - Ability: English(International) - Expert What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.You will be expected to develop clinical study databases by building electronic case report forms and program edit checks as per specifications. Support any updates or changes to the study database (e.g. Protocol amendments) through the change control process. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Detail orientation Ability to establish strong client relationship Roles and Responsibilities: Overall experience of 4+ years with exposure to EDC platforms like Medidata RAVE EDC, Inform, Oracle Clinical, Veeva etc. preferred.Extensive experience in database design, edit check programming, custom function programming and unit testing.Experienced in various modules such as IVRS/RWS integration and Lab administration. Medidata RAVE study builder certified preferred.

Internal/extrernal stakeholders, project team members, vendors 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 Minimum Requirements: Bachelor s degree in statistics, biostatistics, mathematics, computer science or life sciences required. At least 3 years programming experience in industry recommended. For US positions: US military experience will be considered towards industry experience. Demonstrated proficiency in using SAS, R or other programming languages to produce derived analysis datasets and TFLs. Understanding of clinical data structure (e. g. CDISC standards) and relational database. Demonstrated skills in using software tools and applications, e. g. , MS office, XML. Demonstrated ability in the handling and processing of upstream data, e. g. , multiple data forms, workflow, eDC, SDTM. Demonstrated ability in providing outputs to meet downstream requirements, e. g. , ADaM, Data Definition Table, e-submission. Have good understanding of regulatory, industry, and technology standards and requirements. Have good knowledge of statistical terminology, clinical tests, medical terminology and protocol designs. Demonstrated ability to work in a team environment with clinical team members. Preferred Requirments: Minimum of 3 years clinical / statistical programming experience within pharmaceutical clinical development Knowledge of the drug development process, clinical trial methodology, statistics and familiarity with global regulatory requirements Experience in other software packages (e. g. R) Experience with the Linux operating system IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs. iqvia. com

Role: Data Acquisition Lead (FSP) Duration: Contract Location: Remote Work timing: IST or UK Hours Job Description: - Serve as the subject matter expert for the planning, set-up, and acquisition of external clinical data at the study level and manage study start up, conduct and close out activities. - Create external data transfer agreements, ensuring external clinical trial data are in alignment with company Standards and specifications to support data integration, analysis, and reporting. - Help and advice in setting up infrastructure for external data, to flow into company Clinical data pipelines. - Responsible for validation of all 3rd Party Data generated in clinical trial into company Clinical Data pipelines. - Develop strong and productive working relationships with key stakeholders like Clinical Data Management, Clinical Data Engineering, Standards and other Study Execution Team members. - Participate in preparing function for submission readiness and may represent Clinical Trial Tools & Technologies (CT3) group in a formal inspection or audit. - Representing company in interactions with key external partners as part of company CT3 3rd Party Data Acquisition team. - Responsible for timely submission and on-going maintenance of study related 3rd Party Data Acquisition documentation in TMF. - Follow procedural documents and participating in reviewing and updating documents to make sure they are reflective of industry standards and regulatory requirements and include optimal processes. - Liaise with and reviewing work delivered by external partners (e.g. laboratories, eCOA providers, technology providers, etc.) performing services on behalf of company. - Escalate issues to CT3 leadership appropriately. Technical/Functional Expertise: - Working knowledge and understanding of FDA and ICH regulations and industry standards and quality control principles. - Experience with all phases of drug development. - Solid Experience in handling Clinical data acquisition and management from external/3rd Party vendors. - May lead study level negotiation and agreement for data transfer or integration on behalf of company. - Should be able to function collaboratively (with some guidance) with all levels of employees , moderate supervision required. - Knowledge on FTP tools like GlobalScape, Clinical platforms like Veeva CDMS, Elluminate and Veeva TMF will be a plus. Thanks & Regards: Abhinav Krishna Srivastava Mob : +91- 9667680709 FCS Software Solutions Ltd. Email: asrivastava@fcsltd.com

The job responsibilities include two roles Project Standards Manager (PSM) will manage the activities associated with the consistent implementation of global clinical data standards for BMS projects and studies Global Standards Manager (GSM) will assist in the leadership of the development and maintenance of BMS s global clinical data standards and related supportive processes Each individual can perform PSM, GSM or a combination of the two roles. Development, maintenance and Implementation of BMS clinical data Standards Participate in the development and maintenance of global clinical data standards, including operational (CRF and non-CRF) CDISC Study Data Tabulation Model (SDTM), controlled terminology, non-CRF standard data mappings (e.g., lab or ECG), and other applicable industry standards. This could include creation of the metadata and mappings between the standards (operational and SDTM), and documentation of the use of the standard. Participate in relevant study team meetings as standards SME and provide input for standards components, such as CRF design, CRF Completion Guidelines, Programmed edit checks, Data transfer specifications, SDTM mapping specifications and SDTM annotated CRF. Act as an expert on operational data standards, SDTM and/or Analysis Data Model (ADaM) standards, and Clinical Data Interchange Standards Consortium (CDISC) controlled terminology. Act as a consulting resource for study teams regarding the validation of SDTM domains, which may include output from industry standard software tools and BMS custom validation programs. Work with standards management systems and software, such as Metadata Repository, Change Request systems, SDTM validation systems, and issues tracking systems, in the development of systems and processes for creation and maintenance of data standards, including specifications, mappings between standards, and checking adherence to these data standards. Coach CROs and vendors on BMS data standards and related processes Communicate and reinforce content and interpretation of BMS data standards to project and study teams, to ensure consistency in understanding and implementation of standards across a project. Standards Governance Organization and submissions support Process clinical data change requests for new or existing metadata, including developing a Standards manager recommendation and implementation plan for the standard, as applicable, and ensuring that the request is processed through the appropriate levels of the CDSGO Participate in the committees of the CDSGO, partner with functional area stewards, organizing standards topics to be reviewed and ensuring decisions are made in a timely manner, documented in meeting minutes and other forms, and implemented. Provide input and information to facilitate key discussions and decisions regarding standards use and implementation. Provide guidance to Study Teams and Submission Teams on SDTM standards and related submission requirements, (e.g., SDTM annotated CRF, define.xml/pdf, Reviewer s Guide, XPT files). Participate in Study / Submission team meetings, as applicable. Other Key Activities Participate in the development of CDSI or cross functional SOPs, Working Procedures, Guidance documents, and job aids. Participate in the identification, review, evaluation, and implementation of new technologies related to data standards. Develop training materials and provide training on CDS-developed processes. May coach more junior personnel or contract staff, as required Participate in strategic initiatives, special projects, and working groups contributing to business decisions and process changes Identify and propose process improvements while maintaining a strategic focus. Share new industry standards, best practices with project and study teams, and within department as required. Degree Requirements Bachelor s degree required Experience Requirements At least 7 years of relevant industry experience with clinical trials, preferably with clinical data standards as a focus. Experience in Industry Standards (e.g. CDISC) in either the collection (CDASH), tabulation (SDTM) or analysis (ADaM) models. Experience with Medidata Rave(EDC) and Metadata Repository (MDR) is preferred. Experience interpreting Health Authority regulations with a strong compliance background. Strong working knowledge of the overall pharmaceutical development process. Strong working knowledge of SDTM and the creation of data mapping specifications and annotated CRFs. Knowledge of requirements of define.xml. Experience in CRF design, query resolution, and general data validation. Good communication skills, high ability to communicate standards related issues, options, and their impact to project teams and within department. Ability to work effectively in a team environment with medical personnel, study managers, project managers, clinical monitors, data managers, programmers, and statisticians

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 dont 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." Qualifications: Bachelors 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. . We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com

Clinical R Programmer - Experienced Professional (5+ Years Experience) Overview: We are looking for an experienced Clinical R Programmer in combination with SAS with 5+ years of combined experience in R & SAS within the clinical research or pharmaceutical industry . The ideal candidate should have expertise in developing and validating ADaM datasets, tables, listings, and figures (TLFs) using R , along with a strong understanding of CDISC standards, clinical trial data processing, and regulatory compliance . Key Responsibilities: R Programming Tasks: Develop and validate ADaM datasets, tables, and listings using R . Work with R data structures (matrices, vectors, lists, data frames) for dataset creation and manipulation. Implement date formatting, character functions, and missing value handling in R. Utilize industry-standard R packages : DPLYR, TIDYVERSE, HAVEN, ADMIRAL, LUBRIDATE, STRINGR - Data manipulation and analysis. GGPLOT2 - Advanced data visualization. Perform dataset validation and comparisons (equivalent to PROC COMPARE in SAS). Debug and optimize R programs for performance and accuracy. Familiarity with R Markdown and R-Shiny for reporting (optional but preferred). Required Skills & Experience: 5+ years of combined experience in SAS and R programming in the clinical research or pharmaceutical domain . Proficiency in R programming for clinical data processing and visualization. Strong understanding of R packages (DPLYR, TIDYVERSE, HAVEN, etc.). Knowledge of CDISC standards (SDTM, ADaM) and regulatory submission requirements. Experience in debugging, dataset comparisons, and handling missing values in both R and SAS. This role is perfect for professionals looking to leverage both SAS and R programming skills in clinical research, ensuring compliance with industry standards and regulatory requirements . Send your Resume on [email protected] Job Category: Client Based - Sourcing Job Type: Full Time Job Location: Bangalore Chennai Remote