Site Activation Specialist 1
IQVIA · Bangalore, India
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
IQVIA seeks a Site Activation Specialist to coordinate clinical trial site preparation and regulatory activities across assigned studies. The role involves managing documentation, tracking progress, and serving as primary contact between investigative sites, project teams, and internal stakeholders while ensuring compliance with procedures and timelines.
What they're looking for
- Bachelor's degree in life sciences or related field
- 3+ years clinical research experience or equivalent combination of education and experience
- 1+ year experience in a leadership capacity within clinical research
- Knowledge of site activation processes, regulatory requirements, and standard operating procedures
- Proficiency with internal systems, databases, and project tracking tools
What you'll be doing
- Serve as single point of contact between investigative sites, project management, and internal teams for assigned studies
- Execute feasibility assessments, site identification, startup, and activation activities according to regulations and procedures
- Prepare, review, and distribute site documents; ensure accuracy and completeness of deliverables
- Track and follow up on regulatory, ethics, consent forms, and investigator pack approvals aligned with project timelines
- Monitor site performance metrics and provide feedback to management; establish contingency plans as needed
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.