IQVIA, a global leader in clinical research and healthcare analytics, is hiring Site Activation Coordinators for its offices in Thane, Maharashtra and Bangalore, Karnataka. This is an excellent opportunity for Life Science graduates who are passionate about clinical research operations and regulatory documentation.
If you’re detail-oriented, organized, and looking to start your career in clinical trials and site management, IQVIA’s Site Activation Coordinator role is the perfect fit.
🧾 Job Overview
As a Site Activation Coordinator at IQVIA, you will assist in regulatory and start-up activities across clinical study sites. You’ll work under general supervision, collaborating with Site Activation Managers, Project Teams, and Regulatory Staff to ensure smooth and compliant site activation.
🧠 Key Responsibilities
- Perform site activation activities at the country level in compliance with local and international regulations, SOPs, and project timelines.
- Prepare, review, and verify site regulatory documents for accuracy and completeness.
- Track progress of regulatory submissions, ethics approvals, and Informed Consent Forms (ICFs).
- Maintain internal tracking systems, databases, and timelines with updated project information.
- Distribute completed regulatory and contractual documents to internal teams and sites.
- Collaborate closely with cross-functional teams to ensure timely document approvals and investigator pack releases.
🎓 Eligibility & Qualifications
- Required Degree:
- Bachelor’s Degree in Life Sciences, Pharmacy, Biotechnology, or related fields.
- Example degrees accepted: B.Pharm, B.Sc in Life Sciences, Biotechnology, Biochemistry, Microbiology.
- Experience:
- 0–1 year of experience in a healthcare or clinical research environment.
- Freshers with strong documentation and organizational skills are encouraged to apply.
- Skills Needed:
- Strong MS Office and documentation skills.
- Excellent interpersonal communication and coordination abilities.
- Good understanding of the clinical trial process and regulatory requirements.
- Attention to detail and ability to handle multiple projects simultaneously.
💼 Benefits of Working at IQVIA
- Opportunity to work in a global clinical research organization (CRO).
- Exposure to regulatory, clinical, and project management functions.
- Work with a talented team of industry professionals.
- Competitive salary and growth-oriented career path.
- Inclusive work environment promoting innovation and learning.
📍 Job Details
📝 How to Apply
