Clinical Research Coordinator – Join IQVIA in Mumbai!
Summary:
IQVIA, a global leader in clinical research and healthcare intelligence, is seeking a highly motivated and detail-oriented Clinical Research Coordinator (CRC) to join our expanding team in Mumbai. This is an exceptional opportunity for individuals with a background in life sciences, pharmacy, or nursing, and experience in clinical trials, patient management, and regulatory coordination. As a CRC, you will play a vital role in supporting the successful execution of clinical trials from initiation to closeout, ensuring adherence to protocols, ethical guidelines, and regulatory requirements. If you’re passionate about contributing to advancements in healthcare and possess strong organizational and communication skills, we encourage you to apply.
Job Description:
Are you passionate about contributing to the advancement of healthcare through clinical research? Do you thrive in a dynamic environment where your attention to detail and organizational skills can make a real difference? If so, IQVIA invites you to apply for the position of Clinical Research Coordinator (CRC) in Mumbai.
As a CRC at IQVIA, you will be an integral part of our clinical trial operations team, working closely with investigators, sponsors, and other healthcare professionals to ensure the smooth and efficient conduct of clinical trials. You will have the opportunity to contribute to studies across diverse therapeutic areas and gain valuable experience in a leading global organization committed to scientific excellence and high-quality trial execution.
Key Responsibilities:
The Clinical Research Coordinator will be responsible for the following:
- Trial Feasibility & Site Identification: Conducting site and trial feasibility assessments to identify qualified investigators and potential study sites.
- Regulatory Submissions: Compiling essential documents and assisting in the preparation and submission of regulatory documents to relevant authorities.
- Ethics Committee Coordination: Communicating and coordinating with site Ethics Committees to obtain necessary approvals and resolve queries in a timely manner.
- Site Management & Preparation: Overseeing site setup, including pre-screening activities and review of patient databases to identify potential study participants.
- Clinical Trial Supplies Management: Managing clinical trial supplies, including receipt, accountability, storage, and inventory control.
- Study Initiation Visit Preparation: Preparing the site team for study initiation visits and ensuring all necessary resources are available.
- Informed Consent Process: Supporting the informed consent process by educating patients about the study and obtaining informed consent in accordance with ethical guidelines.
- Documentation & Record Keeping: Maintaining accurate and complete site documentation, including study files, patient records, and regulatory documents.
- Sample Collection & Lab Logistics: Overseeing sample collection, processing, and shipment to central laboratories, as well as reviewing lab reports for accuracy and completeness.
- Patient Recruitment Strategies: Implementing patient recruitment strategies to ensure timely enrollment of eligible participants.
- Data Management: Ensuring accurate and timely completion of Case Report Forms (CRFs) and resolving data queries within established deadlines.
- Monitoring Visit Support: Assisting monitors during monitoring visits and audits, providing necessary documentation and addressing any findings.
- Patient Management: Managing patient follow-ups, including scheduling appointments, administering study medications, and providing patient education.
- Reimbursements & Payments: Managing patient reimbursements and payments in accordance with study protocols and guidelines.
- Drug Accountability: Handling drug accountability, including storage, dispensing, and documentation, ensuring compliance with regulatory requirements.
- Site Closeout & Archival: Coordinating for site closeout activities, including archiving essential documents and ensuring proper disposition of study materials.
- Reporting & Communication: Maintaining study logs, manuals, and providing timely reports to stakeholders on study progress.
Qualifications & Skills Required:
- Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Nursing, or a related field.
- Experience in clinical research, including familiarity with ICH-GCP guidelines and site coordination is highly desirable.
- Strong communication, interpersonal, and patient interaction skills.
- Excellent documentation and record-keeping abilities.
- Ability to manage multiple tasks, prioritize effectively, and meet deadlines in a fast-paced environment.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to work independently and as part of a team.
Benefits of Working at IQVIA:
- Global Leadership: Opportunity to work with a global leader in clinical research and healthcare intelligence.
- Diverse Exposure: Exposure to diverse therapeutic areas and large-scale clinical trials, expanding your knowledge and experience.
- Skill Development: Continuous skill development in areas such as compliance, data management, and regulatory processes.
- Career Growth: Opportunities for career growth within clinical operations, project management, and other areas within IQVIA.
- Meaningful Contribution: Make a tangible difference in the lives of patients by contributing to the development of innovative therapies.
- Competitive Benefits Package: Enjoy a competitive salary and benefits package, including health insurance, paid time off, and retirement savings plans.
Join our team and be a part of something meaningful! Apply today!