Site Activation Coordinator
IQVIA is hiring Site Activation Coordinators in Bangalore for its global Clinical Research and Study Start-Up team. This opportunity is ideal for Life Sciences and Pharmacy professionals interested in Clinical Trial Start-Up, Regulatory Documentation, Site Activation, and Clinical Operations.
The selected candidate will work closely with global study teams, Site Activation Managers, ethics committees, and investigative sites to ensure timely study start-up activities and regulatory compliance.
Professionals looking for Site Activation Jobs, Clinical Research Careers, Clinical Operations Roles, and Study Start-Up opportunities should explore this opening.
📋 Job Overview
| Particulars | Details |
|---|---|
| Company | IQVIA |
| Position | Site Activation Coordinator |
| Location | Bangalore, India |
| Experience | Minimum 1 Year |
| Industry | Clinical Research |
| Employment Type | Full-Time |
| Department | Site Activation / Clinical Operations |
| Application Mode | Online Application |
| Application Deadline | 22 June 2026 |
💼 Key Responsibilities
- Perform Site Activation Activities for Clinical Studies.
- Review Site Regulatory Documentation.
- Coordinate with Site Activation Managers and Project Teams.
- Track Regulatory and Ethics Committee Approvals.
- Maintain Study Timelines and Tracking Systems.
- Support Study Start-Up Activities.
- Monitor Investigator Pack Release Documentation.
- Track Informed Consent Form (ICF) Approvals.
- Distribute Regulatory Documents to Study Teams.
- Ensure Compliance with SOPs and Regulatory Requirements.
🎓 Eligibility Criteria
Educational Qualification
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Related Healthcare Disciplines
Experience
- Minimum 1 Year Experience
- Clinical Research Experience Preferred
- Healthcare Industry Experience Accepted
🧠 Required Skills
- Clinical Trial Knowledge
- Site Activation Activities
- Regulatory Documentation
- Study Start-Up Operations
- Clinical Operations
- Documentation Management
- Project Coordination
- Microsoft Office Skills
- Communication Skills
- Stakeholder Management
- Attention to Detail
- Time Management
Clinical Research Career Guide
CRA Interview Quiz
Clinical Trial Assistant Quiz
💰 Salary & Benefits
Based on industry standards for Site Activation and Clinical Operations roles in India:
Estimated Salary Range: ₹5.5 LPA – ₹8.5 LPA
Actual compensation may vary depending on experience, study start-up expertise, and clinical research background.
Employee Benefits
- Global Clinical Trial Exposure
- Hybrid & International Project Opportunities
- Career Growth in Clinical Operations
- Learning & Development Programs
- Health & Wellness Benefits
- Professional Certification Support
- Collaborative Global Work Environment
- Performance-Based Career Progression
🌟 Why Join IQVIA?
- World Leader in Clinical Research & Healthcare Intelligence.
- Exposure to Global Clinical Trial Start-Up Activities.
- Work with International Sponsors and Research Teams.
- Strong Learning and Development Culture.
- Excellent Career Path in Site Activation & Clinical Operations.
- Opportunity to Contribute to Innovative Healthcare Solutions.
- Industry-Leading Technology and Clinical Systems.
- Long-Term Career Stability and Growth.
📈 Career Growth Opportunities
This role can lead to:
- Senior Site Activation Coordinator
- Site Activation Specialist
- Study Start-Up Associate
- Clinical Trial Assistant (CTA)
- Clinical Research Associate (CRA)
- Clinical Operations Specialist
- Study Start-Up Manager
- Clinical Project Manager
📑 Resume Tips for Site Activation Coordinator Roles
- Highlight Clinical Research and Regulatory Documentation Experience.
- Mention Study Start-Up and Ethics Committee Activities.
- Showcase Site Management and Coordination Skills.
- Include ICF, Regulatory Binder, and Essential Document Knowledge.
- Mention GCP and Clinical Trial Compliance Understanding.
- Keep Resume ATS-Friendly and Achievement Oriented.
Before applying, read our complete guide:
Healthcare & Pharma Job Application Guide🎯 Interview Tips for Site Activation Coordinator
Candidates preparing for the IQVIA interview should focus on:
- Clinical Trial Phases and Drug Development Process.
- Site Activation and Study Start-Up Workflow.
- Essential Regulatory Documents.
- Informed Consent Form (ICF) Process.
- Ethics Committee & IRB Approval Process.
- ICH-GCP Guidelines.
- Investigator Site File (ISF) Documentation.
- Clinical Trial Timelines and Milestones.
- Stakeholder Communication Scenarios.
- Behavioral and Situational Questions.
Practice using these resources:
Clinical Research Career GuideCRA Interview Quiz
Clinical Trial Assistant Quiz
📌 How to Apply?
Candidates should prepare an updated resume highlighting Clinical Research experience, Site Activation knowledge, Regulatory Documentation expertise, and Study Start-Up activities.
Before applying, read:
Healthcare & Pharma Job Application Guide🚀 Apply Now
Interested and eligible candidates can apply through the official IQVIA Careers portal.
Apply for Site Activation Coordinator📚 Related Resources from HiTechPlus
❓ Frequently Asked Questions
Q. Who can apply for this role?
B.Pharm, M.Pharm, Pharm.D, B.Sc, M.Sc Life Sciences, and related healthcare graduates with at least 1 year of relevant experience.
Q. Is prior Site Activation experience mandatory?
Clinical Research or Healthcare experience is required, while Site Activation experience is highly preferred.
Q. What is the expected salary?
Approximately ₹5.5 LPA – ₹8.5 LPA depending on experience and qualifications.
Q. What are the major responsibilities?
Site activation, regulatory documentation, ethics approvals, study start-up activities, and clinical trial coordination.
Q. What career opportunities can this role lead to?
CRA, Site Activation Specialist, Clinical Operations Specialist, Study Start-Up Manager, and Clinical Project Manager roles.
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