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Clinical Trial Coordinator I
Remote (India)
1–2 Years
Clinical Research
🏢 About Thermo Fisher Scientific
Thermo Fisher Scientific is a global leader in clinical research and life sciences, supporting pharmaceutical companies in drug development, clinical trials, and laboratory solutions.
📋 Job Overview
- Role: Clinical Trial Coordinator I
- Location: Remote (India)
- Experience: 1–2 Years
- Qualification: Life Sciences / Pharmacy
- Type: Full-Time
📌 Key Responsibilities
- Coordinate clinical trial activities
- Maintain eTMF & audit readiness
- Support CTMS & trial systems
- Manage study documentation
- Track compliance & training
- Prepare reports & meeting minutes
- Handle ISF & site documentation
🎓 Eligibility Criteria
- B.Pharm / M.Pharm / BSc / MSc
- 1–2 years clinical research experience
- Knowledge of ICH-GCP
- Experience with CTMS / eTMF
💰 Salary & Benefits
- ₹4.5 – ₹7.5 LPA
- Work From Home
- Global exposure
- Career growth opportunities
🎯 Why This Role is Important
- Core role in clinical trials
- Strong career path → CRA / PM
- High-demand domain
📚 Internal Resources (Must Read)
🎯 Interview Tips
- Revise ICH-GCP guidelines
- Understand clinical trial phases
- Learn TMF & CTMS basics
- Prepare documentation questions
📚 Practice:
📌 Note Before You Apply:
Ensure you have basic clinical trial knowledge before applying.
Ensure you have basic clinical trial knowledge before applying.
🚀 Job Application Link
📌 Important Note Before You Apply:
Kindly read the full job description carefully before applying. Ensure your profile and qualifications align with clinical trial tracking, study site coordination support, Trial Master File (TMF/eTMF) documentation maintenance, investigator site communication, and ICH-GCP regulatory guidelines compliance standards before proceeding with your application on the Thermo Fisher portal.
Kindly read the full job description carefully before applying. Ensure your profile and qualifications align with clinical trial tracking, study site coordination support, Trial Master File (TMF/eTMF) documentation maintenance, investigator site communication, and ICH-GCP regulatory guidelines compliance standards before proceeding with your application on the Thermo Fisher portal.
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