Thermo Fisher Scientific, through its PPD® clinical research services, is hiring for multiple roles including Clinical Research Associate (CRA I, CRA II, Sr. CRA) and Senior Clinical Trial Coordinator (CTC II). These roles offer a chance to work on global clinical trials, ensuring compliance with ICH-GCP and helping deliver life-changing therapies.
If you’re looking for a career in clinical research in India, these openings provide the perfect opportunity to grow with one of the world’s leading clinical research organizations.
🔹 Job 1: Clinical Research Associate (CRA I, CRA II, Sr. CRA)
Location: Remote/Onsite, India
Work Schedule: Standard (Mon–Fri)
Key Responsibilities
- Monitor investigator sites using risk-based monitoring and root cause analysis.
- Ensure compliance with study protocol, ICH-GCP, SOPs, and regulatory requirements.
- Conduct site initiation, monitoring, and close-out visits.
- Verify data accuracy through SDR, SDV, and CRF review.
- Manage essential documents and maintain audit readiness.
- Facilitate communication between sites, sponsors, and project teams.
- Prepare monitoring reports, letters, and status updates.
Qualifications
- Bachelor’s degree in Life Sciences / Registered Nursing certification.
- Minimum 2+ years’ experience as a clinical research monitor.
- Strong knowledge of ICH-GCP and clinical trial regulations.
- Excellent communication, critical thinking, and organizational skills.
- Proficiency in MS Office and CTMS tools.
🔹 Job 2: Senior Clinical Trial Coordinator / Clinical Trial Coordinator II
Location: Remote, India
Work Schedule: Second Shift (Afternoons)
Key Responsibilities
- Provide administrative and technical support to project teams.
- Maintain study documents, trackers, and systems (Veeva Vault, eTMF, CTMS).
- Coordinate regulatory document reviews and submissions.
- Assist with site files, pharmacy binders, and translation QC.
- Support RBM activities and global project managers.
- Organize and document project meetings.
Qualifications
- Bachelor’s degree preferred.
- 4+ years’ experience as a Clinical Trial Coordinator.
- Experience with Veeva Vault, eTMF, CTMS, global trials.
- Strong organizational, analytical, and multitasking skills.
- Excellent English communication and presentation skills.
✅ Benefits of Working at Thermo Fisher Scientific
- Opportunity to contribute to global clinical trials.
- Career growth in a world-leading CRO environment.
- Collaborative, flexible, and supportive workplace.
- Exposure to cutting-edge digital and decentralized trial models.
📌 How to Apply
Application Link for CRA (Level I, Level II and Sr CRA)
Application Link for Sr Clinical Trial Coordinator / Clinical Trial Coordinator II
