IQVIA, a global leader in clinical research services and healthcare intelligence, is inviting applications for the position of Site Activation Coordinator in Bangalore, India. This full-time opportunity is ideal for life sciences graduates with experience in clinical research, site activation, regulatory documentation, and study startup activities.
The IQVIA Site Activation Coordinator job in Bangalore offers candidates an opportunity to work with global clinical trial teams and contribute to the development of innovative medicines and healthcare solutions. Professionals seeking clinical research jobs in India, site activation coordinator jobs for life sciences graduates, and IQVIA careers in Bangalore should consider this opportunity.
About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company combines data science, advanced analytics, and domain expertise to accelerate medical innovation and improve patient outcomes worldwide.
Job Responsibilities
As a Site Activation Coordinator at IQVIA, you will:
- Perform site activation activities for assigned clinical studies.
- Prepare and review site regulatory documents for completeness and accuracy.
- Coordinate with Site Activation Managers (SAM), project teams, and other departments.
- Inform internal teams regarding completion of regulatory and contractual documentation.
- Distribute completed documents to investigative sites and project team members.
- Maintain internal systems, databases, project timelines, and tracking tools.
- Review and monitor approvals and execution of regulatory and ethics documents.
- Track progress of Informed Consent Forms (ICF) and Investigator Pack (IP) release documentation.
- Support study startup activities in accordance with SOPs and international regulations.
Qualifications Required
Educational Qualification
- Bachelor’s Degree in Life Sciences or a related field.
Experience
- Minimum 1 year of experience in a healthcare, clinical research, or related environment.
Required Skills
- Good understanding of the clinical trial environment and drug development process.
- Strong interpersonal and communication skills.
- Excellent organizational and documentation abilities.
- Proficiency in Microsoft Office applications.
- Strong attention to detail and accuracy.
- Ability to manage multiple projects simultaneously.
- Capability to establish effective working relationships with internal and external stakeholders.
Why Join IQVIA?
- Opportunity to work with one of the world’s leading clinical research organizations.
- Exposure to global clinical trial operations and study startup activities.
- Collaborative and inclusive work environment.
- Career growth opportunities in clinical operations and site activation.
- Competitive compensation and employee benefits package.
- Opportunity to contribute to healthcare innovations that improve patient outcomes globally.
Estimated Salary
Based on industry standards for Site Activation Coordinator roles in India, the expected salary range is:
₹5.5 LPA – ₹8.5 LPA
Actual compensation may vary depending on experience, qualifications, and internal company policies.
How to Apply
