IQVIA, one of the world’s most trusted clinical research organizations, is now hiring a Senior Site Activation Coordinator for its Bangalore, India location. This is an excellent opportunity for life science graduates to join a global team driving site activation, regulatory submissions, ethics approvals, and clinical trial start-up operations.
If you are looking for a career in clinical research, site activation, regulatory operations, or clinical trial management, this role provides unmatched exposure across multiple therapeutic areas and cutting-edge technologies.
Key Responsibilities
As a Senior Site Activation Coordinator, you will:
- Manage country-level site activation activities for clinical studies.
- Perform feasibility checks, site-selection support, and start-up documentation.
- Prepare, review, and track essential study documents including:
- Confidentiality Agreements (CDAs)
- Regulatory submissions
- Ethics committee packages
- Informed Consent Forms (ICFs)
- Investigator Pack release documents
- Coordinate with Site Activation Managers and Project Management teams.
- Ensure compliance with ICH-GCP, SOPs, local regulations, and project-specific requirements.
- Maintain internal CTMS, tracking tools, and project databases accurately.
- Support site maintenance activities when needed.
Required Qualifications
To be eligible for this role, candidates must have:
- Bachelor’s Degree in Life Science or related field.
- Minimum 2 years of work experience, with at least 1+ year in healthcare, clinical research, or a similar domain.
- Strong communication, interpersonal, and organizational skills.
- Ability to manage multiple projects simultaneously.
- Detail-oriented approach and ability to work in cross-functional environments.
Why Join IQVIA?
IQVIA offers a high-growth, innovation-driven work culture that empowers clinical research professionals worldwide. Benefits include:
- Exposure to 21+ therapeutic areas.
- Work with teams across 141 global locations.
- Opportunities to leverage innovative tech platforms and analytics tools.
- Continuous learning & development in clinical and regulatory workflows.
- Work-from-home flexibility (Home-Based India role).
- A collaborative, mission-driven environment improving global patient health.
How to Apply
