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