1120 Clinical Research Jobs - Page 43

Hi We are Hiring Leading ITES Company for Medical Reviewer Role. Please go through the JD and Apply Job Description: Author a company clinical comment (CCC) for case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Edit the Periodic Report Comment, if applicable, directly within the Periodic Report Comment field in the Patient Safety database. Perform the following actions within the Comments field of the GSP Review Workflow step in the Patient Safety database: -Review and respond to any queries/comments from the Case Owner, which are recorded in the Comment field of the GSP Review Workflow step in the Patient Safety database. -Detail any requests for changes to the case, including the narrative. -Detail any follow-up information that is required and not already noted within the Query Manager in the Patient Safety database. Provide product advice as required, especially with regards to case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Review the company causality assessment provided by Medical Advisor. Review the medical sense including seriousness and coding of the case in the global context of the drug or clinical project, including the narrative, AE/SAE terms, suspect drugs, concomitant medications, laboratory data, and medical history. To provide documentation of the review and case comments in Sapphire in Medical Review workflow. Ensure compliance with global and local procedural documents and local implementation of client Maintain knowledge of the marketed drug currently under litigation. Maintain knowledge of the company disease and therapeutic areas for marketed drugs and drugs in development through periodic medical review training held by client medical staff. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Nagpur Search : Job Code # 49 b) For Position in Gandhinagar Search : Job Code # 50 c) For Position in Bangalore Search : Job Code # 51

We are Hiring for Leading ITES Company for Medical Reviewer Profile Pls Apply, We shall call back the relevant profiles. Experience :- Min 1 years of experience in Medical Reviewer domain Job Description for Medical Reviewer Author a company clinical comment (CCC) for case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Edit the Periodic Report Comment, if applicable, directly within the Periodic Report Comment field in the Patient Safety database. Perform the following actions within the Comments field of the GSP Review Workflow step in the Patient Safety database: -Review and respond to any queries/comments from the Case Owner, which are recorded in the Comment field of the GSP Review Workflow step in the Patient Safety database. -Detail any requests for changes to the case, including the narrative. -Detail any follow-up information that is required and not already noted within the Query Manager in the Patient Safety database. Provide product advice as required, especially with regards to case reports that are Suspected Unexpected Serious Adverse reaction (SUSAR). Review the company causality assessment provided by Medical Advisor. • Review the medical sense including seriousness and coding of the case in the global context of the drug or clinical project, including the narrative, AE/SAE terms, suspect drugs, concomitant medications, laboratory data, and medical history. To provide documentation of the review and case comments in Sapphire in Medical Review workflow. • Ensure compliance with global and local procedural documents and local implementation of client. Maintain knowledge of the marketed drug currently under litigation. Maintain knowledge of the company disease and therapeutic areas for marketed drugs and drugs in development through periodic medical review training held by client medical staff. Skills required: Computer Literate (good knowledge of MS Office) Sound understanding of the Drug Safety and Regulatory process Good problem solving and decision-making skills Capability to lead by motivation and example Ability to prioritize schedule and organize Excellent interpersonal and communication skills To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Job Code # 47 b) For Position in Pune Search : Job Code # 48 c) For Position in Nagpur Search : Job Code # 49

Hi, We are hiring for the leading ITES Company for EDC (Veeva & Inform Programmer) Role. JOB DESCRIPTION: Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process Create edit check specifications and program or modify checks at study level within EDC Setup different instances of study URL (e.g.: UAT (User Acceptance Testing), production, testing etc.,) Setup and configure user accounts for study teams Setup and manage blinded and unblinded study configurations Be the SME (Subject Matter Expert) for all database related activities Setup, configure, unit test and functionally validate and integrate other modules within the EDC ecosystem such as coding, integration of IRT, safety system, local labs etc., Familiar with custom functions within EDC systems Work closely with EDC vendors regarding any tool related issues in the system Ability to troubleshoot database setup as per study needs Prepare, test and implement postproduction changes as per study needs Archive and retire the study URL after database lock Partner with appropriate team members to establish technology standards and governance models • Establish and support business process SOPs. Oversee system delivery life cycle in collaboration with appropriate partners including Clinical Operations, Clinical Supplies, IT (Information Technology), and Quality organizations Be a primary change agent to ensure adoption of new capabilities and business process Be the contact for Clinical Technology vendors to ensure established milestones are met with the highest degree of quality. Work with leaders to resolve issues affecting the delivery of clinical trials Collaborate with standards team in creating standard CRF libraries for study level consumption Work closely with data engineers and data management programmers at study level integration and delivery Lead technology vendor oversight activities. Be a process expert for operational and oversight models. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Job Code # 181 b) For Position in Pune Search : Job Code # 182 C) For Position in Bangalore Search : Job Code # 183

Hi We're hiring for Leading ITES Company for EDC (Veeva Programmer) Role Experience in EDC & Veeva is Must. Job Description : Create eCRF specifications, design, develop and unit test and functionally validate clinical trial setup process Create edit check specifications and program or modify checks at study level within EDC Setup different instances of study URL (e.g.: UAT (User Acceptance Testing), production, testing etc.,)) Setup and configure user accounts for study teams Setup and manage blinded and unblinded study configurations Be the SME (Subject Matter Expert) for all database related activities Setup, configure, unit test and functionally validate and integrate other modules within the EDC ecosystem such as coding, integration of IRT, safety system, local labs etc., Familiar with custom functions within EDC systems Work closely with EDC vendors regarding any tool related issues in the system Ability to troubleshoot database setup as per study needs Prepare, test and implement postproduction changes as per study needs Archive and retire the study URL after database lock Partner with appropriate team members to establish technology standards and governance models Establish and support business process SOPs. Oversee system delivery life cycle in collaboration with appropriate partners including Clinical Operations, Clinical Supplies, IT (Information Technology), and Quality organizations Be a primary change agent to ensure adoption of new capabilities and business process Be the contact for Clinical Technology vendors to ensure established milestones are met with the highest degree of quality. Work with leaders to resolve issues affecting the delivery of clinical trials Collaborate with standards team in creating standard CRF libraries for study level consumption Work closely with data engineers and data management programmers at study level integration and delivery Lead technology vendor oversight activities. Be a process expert for operational and oversight models. Partner with appropriate team members, technology vendors, and CRO partners to avoid and resolve risks. Confirm archival and inspection readiness of all Clinical Technology Trial Master File (TMF) documents Participate in preparing function for submission readiness and may represent Clinical Information Operations (CIO) group in a formal inspection or audit. Track study deliverables and evaluate study metrics to mitigate risk for major data management deliverables. Adaptable to new ways of working using technology to accelerate clinical trial setup Education and Experience Requirements: Bachelor's degree or related experience. Knowledge of drug development process. Minimum of 4+ years experience in Data Management, Programming, Clinical IT, or other Clinical Research related fields. Hands-on experience with at least one EDC system (e.g.: Medidata Rave, Inform, Veeva etc.,) Experience programming in CQL, working with JSON format and/or C# is preferred Experience integrating other clinical trial modules (e.g.: lab, safety, IRT, coding etc.,) with the EDC system Understanding of industry standard technologies to support Clinical Development needs (e.g., CTMS, SAS, R or Python, Data Warehouses, SharePoint) To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : EDC Veeva & Inform Programmer Mumbai (Job Code # 181) b) For Position in Pune Search : EDC Veeva & Inform Programmer Pune (Job Code # 182) c) For Position in Bangalore Search : EDC Veeva & Inform Programmer Bangalore (Job Code # 183)

Hi, We are hiring for the ITES Company for the Clinical SAS + SQL Programmer Profile. Job Description: Minimum 4 years of experience in any CDMS application. To perform a wide range of Clinical Data Management activities resulting in high quality database within stipulated timelines. To provide expertise in programming concepts to the Data Management team Must be able to develop the connection with the stake holders by pro-actively communicating over the calls and handling the queries by resolving them on the spot or later depending on the nature of the problem. Must be able to contribute the solutions to the DMs or Medical scientist for their New requirements either programmatically or convincing them with the technical limitations, if any, along with providing alternative solution. Must have capability to develop new Macros in SAS or modify any SAS Macros that are used globally throughout studies as a part of automation. Preferred Skills: Excellent interpersonal and communication skills Capability to lead by motivation and exle. Strong knowledge in SAS macros is required. General knowledge of Clinical Trials and Pharmaceutical Industry Oracle/PL SQL, CDMS like SAS, Inform etc Key Skills: a) Minimum 4 years of experience in any Clinical Data Management application. b) Should have Oracle/PL SQL, CDMS like SAS, Inform etc c) Any Medical Graduate To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Pune Search: Job Code # 483 b) For Position in Bangalore Search: Job Code # 484 c) For Position in Hyderabad Search: Job Code # 485

Hi We are hiring for Leading ITES Company for Clinical Data Manager Profile. Role & responsibilities: Candidate should have 2-5 years of experience of CDM with experience in Conduct Scope of work 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 the 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 training 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 Caisis, Rave, CDM (startup, closeout, conduct) Client interaction and meetings. Bringing up new ideas and executing new plans to cope with the backlog. Training new team members as and when required. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Job Code # 205 b) For Position in Pune Search : Job Code # 206 C) For Position in Bangalore Search : Job Code # 207

Hi We are hiring for Leading ITES Company for Clinical Data Manager Profile. Role & responsibilities: Candidate should have 2-5 years of experience of Clinical Data Manage (CDM) with experience in Conduct Scope of work 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 the 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 training 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 Caisis, Rave, CDM (startup, closeout, conduct) Client interaction and meetings. Bringing up new ideas and executing new plans to cope with the backlog. Training new team members as and when required. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Job Code # 205 b) For Position in Pune Search : Job Code # 206 C) For Position in Bangalore Search : Job Code # 207

Hi We are Hiring For Leading ITES Company for the position of PV Aggregate Reporting Role Job Description To perform all pre-DLP activities and planning for all assigned reports as per client instructions and timelines including the conducting of strategy meeting, kick-off meetings and other ad hoc report related meetings. Performs activities related to the preparation, writing and review of safety portions of Periodic To perform compilation of all global and country specific periodic aggregate safety reports assigned by the supervisor. To perform peer review of the assigned periodic safety report and complete the corresponding QC checklists within the assigned timeline. To track and drive the progress of safety periodic reports as per the client defined timelines. To ensure compliance to SOPs (client e-manuals and training modules) and other process related documentation Aggregate Safety Reports (PBRER, DSUR etc.) Eligibility: Minimum 2 - 3 years of medical writing work experience including 1 to 2 years of experience in periodic aggregate safety report writing (i.e. PBRER, PSUR, DSUR etc.) Working knowledge of MS Office applications Flexibility to work as per business requirements. Understands and interprets data/information and its practical application. Knowledge of industry and business principles related to biopharmaceutical products and combination products. Good interpersonal, verbal, and written communication skills To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : PV Aggregate Mumbai (Job Code # 54) b) For Position in Pune Search : PV Aggregate Pune (Job Code # 55)

We are Hiring For Leading ITES Company for the position of PV Aggregate Reporting Role Job Descriptions To perform all pre-DLP activities and planning for all assigned reports as per client instructions and timelines including the conducting of strategy meeting, kick-off meetings and other ad hoc report related meetings. Performs activities related to the preparation, writing and review of safety portions of Periodic To perform compilation of all global and country specific periodic aggregate safety reports assigned by the supervisor. To perform peer review of the assigned periodic safety report and complete the corresponding QC checklists within the assigned timeline. To track and drive the progress of safety periodic reports as per the client defined timelines. To ensure compliance to SOPs (client e-manuals and training modules) and other process related documentation Aggregate Safety Reports (PBRER, DSUR etc.) Eligibility: Minimum 2 - 3 years of medical writing work experience including 1 to 2 years of experience in periodic aggregate safety report writing (i.e. PBRER, PSUR, DSUR etc.) Working knowledge of MS Office applications Flexibility to work as per business requirements. Understands and interprets data/information and its practical application. Knowledge of industry and business principles related to biopharmaceutical products and combination products. Good interpersonal, verbal, and written communication skills To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : PV Aggregate Mumbai (Job Code # 54) b) For Position in Pune Search : PV Aggregate Pune (Job Code # 55)

Hi We are Hiring for ITES Company for the Pharmacovigilance Aggregate Reporting Role Job Description: Minimum 2 - 3 years of medical writing work experience including 1 to 2 years of experience in periodic aggregate safety report writing (i.e. PBRER, PSUR, DSUR etc.) To perform all pre-DLP activities and planning for all assigned reports as per client instructions and timelines including the conducting of strategy meeting, kick-off meetings and other ad hoc report related meetings. Performs activities related to the preparation, writing and review of safety portions of Periodic Aggregate Safety Reports (PBRER, DSUR etc.) To perform compilation of all global and country specific periodic aggregate safety reports assigned by the supervisor. To perform peer review of the assigned periodic safety report and complete the corresponding QC checklists within the assigned timeline. To track and drive the progress of safety periodic reports as per the client defined timelines. To ensure compliance to SOPs (client e-manuals and training modules) and other process related documentation. Drafting and maintaining PV agreements and SDEA'S Workflow management along with case allocation Accountable for updating relevant databases, repositories, trackers and logs on an ongoing basis as per relevant SOPs Submission of cases to various regulatory Authorities (EMA, MHRA, FDA, Health Canada) Execute drug safety data management process- a combination of case intake, triage, case entry, medical coding, narrative writing, peer review, case follow-up, report preparation- with accountability for quality and timelines of deliverables and responsibility for process improvements Maintaining and drafting project level SOPs as per Statement of Work. Create/collate periodic reports for client report meetings. To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : PV Aggregate Mumbai (Job Code # 54) b) For Position in Pune Search : PV Aggregate Pune (Job Code # 55)

Senior Manager, Financial Business Partnering- Chennai ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Manager, Financial Business Partnering to join our diverse and dynamic team. As the Senior Manager in this role at ICON, you will provide strategic financial insights and support to various departments, helping to drive informed decision-making and enhance overall business performance. Your expertise will be vital in fostering collaboration between finance and operational teams. What You Will Be Doing: Leading the financial business partnering function to provide comprehensive financial support and insights to business units. Collaborating with cross-functional teams to develop budgets, forecasts, and financial plans that align with organizational objectives. Conducting financial analysis to evaluate project performance and identify opportunities for cost savings and efficiencies. Preparing and presenting financial reports and recommendations to senior management and stakeholders. Mentoring and developing a team of financial analysts to enhance their skills and foster a high-performance culture. Your Profile: Degree in finance, accounting, or a related field; MBA or professional certification (CPA, CMA) is preferred. Extensive experience in financial business partnering, analysis, and reporting, ideally within the healthcare or clinical research sectors. Strong understanding of financial modeling, budgeting, and forecasting techniques. Exceptional analytical and problem-solving skills, with the ability to translate data into actionable insights. Excellent communication and interpersonal skills, with a proven ability to build relationships and influence stakeholders at all levels. What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirementsWe would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON EmployeePlease click here to apply

Senior Accounts Receivable Associate - India, Trivandrum - Hybrid, Office-Based ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Senior Accounts Receivable Associate to join our diverse and dynamic team. As a Senior Accounts Receivable Associate at ICON, you will play a crucial role in managing and optimizing the accounts receivable processes to ensure the timely and accurate collection of payments. You will contribute to maintaining financial health by overseeing invoicing, collections, and customer account management. What You Will Be Doing: Managing the accounts receivable process, including invoicing, payment collection, and account reconciliation. Collaborating with cross-functional teams to resolve any billing issues or discrepancies and ensure accurate financial transactions. Overseeing the review and analysis of accounts receivable aging reports to identify and address outstanding balances. Providing support and guidance on accounts receivable policies and procedures to ensure compliance and efficiency. Building and maintaining positive relationships with clients and internal stakeholders to facilitate smooth financial operations. Your Profile: Bachelor s degree in Accounting, Finance, or a related field. Proven experience in accounts receivable or a similar financial role, with a strong understanding of invoicing and collections processes. Excellent organizational skills and attention to detail, with the ability to manage multiple tasks and meet deadlines. Strong communication skills, with the ability to effectively interact with clients and internal teams. Proficiency in accounting software and Microsoft Office, particularly Excel, with the ability to analyze financial data and generate reports. What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirementsWe would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON EmployeePlease click here to apply

Job Description Role & responsibilities Clinical Psychologist Assess your Patients needs, abilities and behaviour using standardized psychometric tests, interviews, and direct observation of behavior. Clinical Psychologist is an integral team member of Child Development Centre of Dr.KMH and enthusiastically participates in holistic development of children with special needs. Responsible for conducting Development, behavioural and psychological assessment of children using standardized scales and tools. Plan, monitor and initiate appropriate treatment programmes and interventions including therapy, counselling in collaboration with other team members and colleagues. Ensures meticulous documentation of the assessment, counseling, therapy sessions and progress of the patient. Evaluate the efficacy and outcome of treatment. Counselling and support to caregivers, parents, and family members. Partcipates in education programmes,,clinical meetings and workshops to enhance professional development and update methodology and techniques. Actively participates in Social and Community welfare programmes of the Institution pertaining to mental health. Implement and participate in Clinical research projects. Preferred candidate profile Qual: M Phil Clinical Psychologist. Doctoral degree in clinical psychology. Registered with HCPC. Experienced with specialist psychological assessment and treatment of a wide range of mental health problems of varying severity and complexity. Proficient with psychological therapies, risk assessment, training, and supervision. Proficient with planning and performing psychological interventions. Current awareness of developments in relevant fields. Ability to maintain and complete clinical documentation consistently. Perks and Benefits As per Market Standard

Customer Service Rep _ Office Based _ Chennai/Trivandrum ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Customer Service Rep to join our diverse and dynamic team. As a Customer Service Rep at ICON, you will play a pivotal role in providing exceptional support to our clients and stakeholders, ensuring their needs are met and enhancing their experience with our services. What you will be doing Responding promptly to customer inquiries via phone, email, or chat Providing accurate information about our products, services, and clinical trial processes Assisting customers with order placement, account management, and issue resolution Liaising with internal teams to address customer concerns and escalate complex issues as needed Maintaining detailed records of customer interactions and transactions Your profile High school diploma or equivalent; bachelors degree preferred Proven experience in customer service or a related field Excellent communication and interpersonal skills Strong problem-solving abilities with a customer-centric approach Ability to multitask, prioritize, and manage time effectively What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirementsWe would encourage you to apply regardless - there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON EmployeePlease click here to apply

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. The System Validation Services (SVS) team supports and improves the compliance of the company’s technology solutions and technology solution offerings by standardized, harmonized, and streamlined validation/qualification activities based on the current GxP requirements and risk management principles. Support efforts to define, adopt, and oversee compliance to processes and standards as the fundamental baseline for Infrastructure Life Cycle, Software Development Life Cycle, Technology Quality Life Cycle and delivery. Supports efforts, in collaboration with the business to monitor, identify and implement continuous process improvement across all technology business units. Supervise and ensure the effective implementation of technology solutions for quality management, aiding in delivering products and services to customers. Offer expertise to ensure technology solution projects comply with established standards. Key Accountabilities: Accountability Validation Representative Lead specific tasks for executing Parexel system’s validation strategy. Plan and oversee a risk-based approach to the validation of Parexel systems, in support the Technology Solution Validation Team. Support the provision of validation consultancy, guidance and oversight to ensure compliance with applicable regulatory and quality requirements, and applicable Policies and SOPs. Conduct Periodic Reviews to verify the validated state of each technology solution has been maintained and report findings. Support risk management activities to identify, assess, and control technology-related risks eliminating risks or reducing risks to an acceptable level. Assist with logistical support and initial planning for audit/inspection hosts and provides standard presentation for covering Infrastructure Life Cycle, Software Development Life Cycle and Technology Quality Life Cycle in audit. Assists audit/inspection hosts with data collection and initial collation for the responses. Support activities for development of risk management processes in line Assist with data collection and initial review of Requests For Information (RFI). Performs general and administrative tasks including accurate and timely completion of timesheet. Standards & Quality Framework Assists Process Owners and Stakeholders to support the design, development, implementation, and maintenance of Validation Framework Controlled Documents. Contribute to the development and maintenance of Managed Information and guidance in support of the Validation Framework. Contribute to the development and delivery of training material in support of the Validation Framework. Skills: Entry/mid-level experience in computer technology quality and compliance (including computerized system validation) and the pharmaceutical industry across multiple disciplines within Clinical Drug Development (Phase I/II/III/IV) and/or Manufacturing. Basic knowledge of continuous improvement methodologies. Exhibits competency across core project management activities. Excellent interpersonal, verbal and written communication skills, business understanding, negotiation skills and strong organizational skills. High ability to work in a customer-focused, fast-paced and rapidly changing environment with the high ability to prioritize workload and manage multiple and varied tasks with enthusiasm and some supervision. Highly motivated, seeks opportunities for development, client-focused, having the ability to work with guidance on own initiative. Exhibits a sense of urgency when addressing problems and ensures completion of commitment. Culturally aware and ability to think and work globally. Intermediate desktop software skills (MS Office, Excel, Adobe PDF etc.). Knowledge and Experience: Entry/mid-level Clinical trials and / or Clinical trials and /or research work experience required, with emphasis on GCP and technology compliance. Familiar in technology as it relates to clinical trial activities, including System Life Cycle process and applicable GCP regulations pertaining to Computer Systems. Entry knowledge of project management, Lean Six-Sigma, auditing and/or risk management methodologies. Education: Educated to degree level (technology, biological science, pharmacy or other health related discipline preferred) or equivalent qualification, or 3+ years clinical research experience.

Site identification Confirming availability of implants at site Site staff training, patient information sheet, consent form, trial master file, product description, logs/ source document, Clinical trial document Arrangement of demonstration Required Candidate profile Any Medical/ Biomedical or related field graduate with Min. 5 years of relevant experience, currently working as a CRA with Medical Device industry, Excellent communication and pleasing personality

We are seeking a skilled and detail-oriented Medical Content Writer to join our team. The ideal candidate will be responsible for creating accurate, engaging, and well-researched medical and healthcare content tailored to a variety of audiences including healthcare professionals, and industry stakeholders. Research and write clear, concise, and evidence-based medical content for articles, blogs, newsletters, white papers, brochures, and social media. Ensure all content is scientifically accurate, compliant with industry regulations, and aligned with the latest clinical guidelines. Edit and proofread content for clarity, grammar, and medical accuracy. Stay updated with current healthcare news, medical breakthroughs, and trends in the healthcare industry. Optimize content for SEO and digital platforms when required. Requirements: Bachelor's or Masters degree in Life Sciences, Medicine, Pharmacy, Nursing, or a related field. (Medical writing certifications are a plus.) Proven experience in medical or scientific writing. Strong research skills and the ability to synthesize complex data from multiple sources. Excellent writing, editing, and proofreading skills with attention to detail. Working Days - 6 Days (Last Saturday & all Sundays are off) Working Timings - 10 AM to 6 PM

We Are Hiring || IVR Clinical Reviewer || Hyderabad || Up to 7 LPA|| HR SWETHA 9030360584|| Exp :- Min 1+ years exp as a Clinical reviewer into IVR Only Experienced certified coders Package :-Up to 7LPA Locations :- Hyderabad Work from office Reliving is Mandatory Notice period: Prefers Immediate joiners- 30 days Interested candidates can share your updated resume to HR SWETHA 9030360584 share resume via WhatsApp ) Refer your friend's / Colleagues

We are seeking an experienced and detail-oriented Clinical Research Lead to oversee the planning, execution, and management of clinical trials across all phases (IIV), with a particular emphasis on infectious disease studies. The successful candidate will play a pivotal role in protocol development, regulatory compliance, and cross-functional leadership to ensure the successful delivery of clinical research programs. Key Responsibilities: Lead and manage clinical trials from Phase I through Phase IV, ensuring timelines, budgets, and quality standards are met. Provide scientific and strategic input into clinical trial design, execution, and data analysis. Develop, review, and finalize clinical trial protocols, investigator brochures, informed consent forms, and other essential documents. Serve as the primary point of contact for internal and external stakeholders including investigators, CROs, and regulatory agencies. Oversee site selection, initiation, monitoring, and closeout activities. Ensure compliance with GCP, ICH guidelines, regulatory requirements, and company SOPs. Collaborate with cross-functional teams including regulatory affairs, biostatistics, medical writing, and data management. Monitor and assess study performance metrics and implement corrective actions when necessary. Provide mentorship and guidance to junior clinical team members. Stay current with industry trends, emerging infectious disease threats, and evolving regulatory environments. Qualifications: Advanced degree in Life Sciences (Ph.D, MBBS, MD, Minimum 5–8 years of experience in clinical research, with at least 3 years in a leadership role. Demonstrated experience managing clinical trials in all phases (I–IV) . Strong background in infectious disease clinical studies. Proven expertise in clinical protocol development and regulatory submissions. Excellent organizational, communication, and leadership skills. Ability to work independently and manage multiple projects in a fast-paced environment.

Urgent Requirements for Medical Transcriptionist Exp : 1 to 5yrs Salary : Upto 40k max Location : Bangalore Work from office Night shift Good communication skills Interested candidates send CV to Dharshan03110@gmail.com

Designs, develops, and enhances cloud-based, SaaS web-based clinical trials applications Collaborates with product, engineering, and software quality assurance (SQA) team members for integration, design, and verification in an agile environment Adheres to best practices and Emmes quality standards for code security, optimization, and reusability Uses established frameworks for a seamless user experience across platforms Performs unit testing, debugging, and troubleshooting as needed to ensure quality of work Performs code reviews, assesses regression impact for design changes, and completes technical documentation Identifies opportunities for refactoring/reworking major modules and sees implementation through to deployment Mentor and coach junior and mid-level developers, promoting a collaborative and learning-driven environment Conduct regular code reviews, provide feedback, and foster a culture of continuous improvement Encourage the team to experiment with new technologies, techniques, and methodologies Overview Emmes Group: Building a better future for us all Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience We believe the work we do will have a direct impact on patients lives and act accordingly We strive to build a collaborative culture at the intersection of being a performance and people driven company We re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company If you share our motivations and passion in research, come join us! Primary Purpose Designs, develops, and enhances cloud-based, software-as-a-service (SaaS) web-based clinical trials applications Responsibilities Designs, develops, and enhances cloud-based, SaaS web-based clinical trials applications Collaborates with product, engineering, and software quality assurance (SQA) team members for integration, design, and verification in an agile environment Adheres to best practices and Emmes quality standards for code security, optimization, and reusability Uses established frameworks for a seamless user experience across platforms Performs unit testing, debugging, and troubleshooting as needed to ensure quality of work Performs code reviews, assesses regression impact for design changes, and completes technical documentation Identifies opportunities for refactoring/reworking major modules and sees implementation through to deployment Mentor and coach junior and mid-level developers, promoting a collaborative and learning-driven environment Conduct regular code reviews, provide feedback, and foster a culture of continuous improvement Encourage the team to experiment with new technologies, techniques, and methodologies Qualifications 6 or more years of related professional experience Min 4 years of experience in ReactJS and JavaScript/Typescript Min 4 years of experience in web platform development tools like Node js, Express, AWS Amplify, AWS Lambda, AppSync, and GraphQL Min 4 years of experience in working with any relational or No SQL database Min 2 years of experience in leading a team of engineers Expertise in developing Single Page Applications (SPA) Expertise with authentication and data caching Expertise in API security Expertise with DynamoDB, Amazon Aurora, or other relational database management system Experience with source code repositories like AWS CodeCommit, Git/GitHub, or SVN Experience working in an agile team CONNECT WITH US! Follow us on Twitter - @EmmesCRO Find us on LinkedIn - Emmes

The Associate Director of CSC Business Capabilities plays a pivotal role in overseeing and optimizing the functions within the Clinical Supply Chain (CSC). The Associate Director leads a team that provides Clinical Supply Chain (CSC) representation for Interactive Response Technology (IRT), Clinical Supply Chain Logistics (CSCL) and Business Operational activities related to CSC budget (IRT, CSCL, and Comparator), contract administration and financial metrics. This position requires a strategic leader capable of managing a team, optimizing budgets, supporting logistical operations in the APAC region and providing IRT study support. Key Responsibilities: Lead, mentor, and oversee a team of Managers and Specialists who support IRT, CSCL, and other CSC business capabilities. Foster a culture of collaboration, innovation, and excellence, encouraging team members to achieve their full potential. Business support for CSC operational activities: Assist the Director of Clinical Integration and Enablement (CI&E) with compiling, maintaining, and monitoring the CSC portion of the R&D portfolio budget (inclusive of IRT, Logistics, and Comparator support) to achieve established CSC R&D Savings Targets. Provide input into monthly budget projections and contribute to the preparation of formal corporate projections. Oversee contracts administration, financial metrics and ad-hoc reporting for the CSC organization by leading individuals responsible for executing and managing contract activities, ensuring compliance, efficiency, value creation, and adherence to financial targets. Logistical support and Operations Management: Within the APAC region, oversee operations across a network of distribution centers, ensuring compliance with all applicable regulations and supporting the distribution needs of BMS clinical trials for Investigational Medicinal Products (IMPs). Support the collection of relevant metrics, conduct analysis to support budget and expense management, vendor performance management, and continuous improvement goals. Oversee Returns and Destruction operations across a network of distribution centers, ensuring compliance with all applicable regulations and supporting the compliance needs of BMS clinical trials for Investigational Medicinal Products. Work with 3rd party and internal partners to monitor and drive returns and destruction reporting, evaluation, trending, and operational activities to reflect the BMS portfolio, business model, and evolving regulations. IRT Study Support and Vendor Management: Ensure an excellent level of support and service is provided by on site IRT personnel to promote seamless execution and alignment with IRT study objectives. Support time zone appropriate departmental audits. Manage vendor contractual obligations in conjunction with Global Procurement through documents such as Master Services Agreement, Quality Agreement, Service Level Agreement, rate cards, etc Additional tasks within scope of expertise and experience as assigned by the supervisor in pursuit of BMS goals. Evaluate and refine operational processes to yield strategic improvements, cost savings and operational efficiencies. Provide regular feedback to division and departmental heads of personnel within IRT, CSCL, and other CSC business capabilities functions. Qualifications: Undergraduate/graduate degree in business, science, supply chain management or related field. Certification in supply chain, clinical research, or logistics (e.g., PMP, Lean Six Sigma, APICS) is preferred. Minimum of 8 years of relevant experience in supply chain operations, logistics, budget management, operational excellence, or related fields in the pharmaceutical or biopharmaceutical industry. Demonstrated ability to lead, mentor, and develop a high-performing team while fostering collaboration and honing individual strengths. Strong interpersonal skills to drive team engagement and lead organizational change initiatives. Proficiency in managing financial operations, budgeting, and contract administration. Expertise in facilitating and overseeing Interactive Response Technology (IRT) studies and systems is highly desirable. Thorough understanding of supply chain logistical systems, including transportation, distribution, returns, and destruction across multiple regions is highly desirable Strong knowledge of clinical trial processes and Investigational Medicinal Products (IMPs) handling. Experience in driving regulatory compliance across functions. Effective conflict resolution and relationship management skills across departments and external partners. Ability to oversee multiple ongoing projects, prioritize timelines, manage resources, and align projects with organizational goals. Advanced organizational skills, negotiation skills and attention to detail. Excellent communication skills, both verbal and written. Proficient with MS Office suite

Position Summary: The Database Programmer II is responsible for the design, development, testing, implementation, maintenance and support of clinical databases and applications. Position will interface directly with the internal team (i.e. Data Management, Project Management, etc.), EDC vendor, clients and third-party vendors to gather requirements and provide status updates. Qualifications: Minimum Required: Must have experience in developing and customizing clinical data management databases in a clinical, scientific or health care discipline 3 years experience in clinical database programming Bachelor s and/or a combination of related experience Medidata Rave EDC Rave API integration experience using external vendor modules Good to have Rave Advanced Custom Function programming experience Other Required: Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook. Able to handle a variety of clinical research tasks. Excellent organizational and communication skills Professional use of the English language; both written and oral. Experience in Object Oriented Programming (C#, C++, VBS, etc. ), scripting language (PERL, etc.), SAS, R, SQL Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.) Experience in clinical database management system development. Experience in a clinical, scientific or healthcare discipline. Experience in utilizing various clinical database management systems Broad knowledge of drug, device and/or biologic development and effective data management practices Strong leadership and interpersonal skills Must be able to communicate effectively in the English language. Preferred: Oncology and/or Orphan Drug therapeutic experience Base SAS , SAS/STAT and SAS/ACCESS software SAS Macro programming language Advanced experience in Database Management, object-oriented programming Veeva set up experience

Liaise with investigator sites to notify of alert values, critical values, data clarifications and data revision requests. Act as primary contact for clinical investigator sites. Resolve issues for study coordinators concerning any aspect of the laboratory services in a timely manner. Facilitate the flow of information between investigator site and Project Management. Liaise with internal stakeholders in order to facilitate the laboratory sampling process. Ensure that Project Management team is made aware of any information that may influence the smooth running of a particular project. Retrieve voicemail messages concerning supply orders, test or document requests, call backs etc. in a prompt manner. Assist with the recruitment and training of new team members. May provide leadership to team in absence of supervisor / manager / equivalent. Provide support during routine or regulatory audit. Mandatory needs: Excellent customer service skills Fluency in one or more foreign language(s) may be required Excellent written and verbal communication skills Good word processing skills Good organizational skills Basic leadership skills Attention to detail Ability to work in a fast-paced environment Ability to establish and maintain effective working relationships with coworkers, managers and clients High school diploma or educational equivalent and 3 years customer service experience; or equivalent combination of education, training and experience . 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 Education (Life Sciences) work includes: Providing field support to both customers and other field personnel Conducting on-site education and consulting, and supports establishment and maintenance of customer relations with healthcare professionals and organizations Participating and developing presentations for conventions, forums, and meetings for the purpose of product awareness Sharing product information/data analysis to clinical research groups Requires education in a health-related field and clinical experience. May have RN or Pharm D.