Looking to build a career in clinical research and site activation? IQVIA is hiring a Site Activation Coordinator for its Bangalore team. This role is ideal for candidates with a life sciences background and experience in clinical trial documentation, regulatory submissions, and site activation processes.
If you’re aiming to grow in clinical operations, regulatory affairs, or CRO roles, this opportunity offers strong exposure to global clinical trial environments.
Job Overview
- Role: Site Activation Coordinator
- Company: IQVIA
- Location: Bangalore, India
- Job Type: Full-time
- Job ID: R1532119
- Application Deadline: April 16, 2026
The Site Activation Coordinator supports clinical trial site activation activities, ensuring compliance with regulatory guidelines, SOPs, and study timelines.
Key Responsibilities
- Perform site activation activities for clinical trials under supervision
- Prepare and review site regulatory documents for accuracy and completeness
- Track and manage ethics approvals, ICF (Informed Consent Forms), and Investigator Pack (IP)
- Coordinate with Site Activation Managers (SAM), project teams, and sponsors
- Maintain clinical trial databases, tracking tools, and timelines
- Ensure proper documentation distribution and compliance
- Follow up on regulatory approvals and document execution
Required Qualifications
- Bachelorโs degree in Life Sciences (B.Pharm, M.Pharm, PharmD, BSc, MSc preferred)
- Minimum 1 year experience in clinical research / healthcare / CRO
- Basic understanding of clinical trial processes and drug development
- Strong communication and organizational skills
- Proficiency in MS Office (Word, Excel, PowerPoint)
- High attention to detail and ability to manage multiple projects
Preferred Skills
- Knowledge of site activation and regulatory documentation
- Familiarity with clinical trial systems and SOPs
- Ability to collaborate with cross-functional teams
Salary & Benefits
- Estimated Salary: โน3.5 โ โน6 LPA
- Opportunity to work with a global CRO leader
- Exposure to international clinical trials
- Career growth in clinical operations & regulatory affairs
- Professional and structured work environment
Why Join IQVIA?
IQVIA is a global leader in clinical research services and healthcare intelligence, helping accelerate drug development and patient outcomes. Working here provides:
- Global project exposure
- Strong career progression in clinical research
- Learning opportunities in site activation & regulatory processes
How to Apply
