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Hiring Clinical Trial Coordinator
🏢 Thermo Fisher Scientific
📍 Mumbai / Remote
⏳ Freshers
📊 Clinical Trials
Thermo Fisher Scientific is hiring Clinical Trial Coordinator I (FSP) for freshers. This is a remote clinical research job with global exposure in clinical trial operations, site activation, and regulatory support.
👉 Explore career path: Clinical Research Career Guide
📋 Job Overview
- Role: Clinical Trial Coordinator I
- Experience: 0–1 Years (Freshers eligible)
- Qualification: Life Sciences / Pharmacy / Biotech
- Location: Mumbai / Remote
- Type: Full-Time
📌 Key Responsibilities
- Support clinical trial operations and coordination
- Manage eTMF and investigator file review
- Assist in site activation & regulatory submissions
- Maintain CTMS and clinical systems
- Handle documentation and tracking
- Support audit readiness and compliance
- Coordinate with global teams and sponsors
💻 Required Skills
- Knowledge of ICH-GCP guidelines
- Strong documentation & communication skills
- MS Office (Excel, Word, PowerPoint)
- Time management & multitasking
- Attention to detail
🎓 Eligibility
- B.Pharm / M.Pharm / Pharm.D / BSc / MSc
- Biotech / Life Sciences background
- Freshers can apply
🌟 Why Apply?
- 100% Remote job opportunity
- Work on global clinical trials
- Strong career growth in clinical research
- Exposure to CRO environment
💡 Interview Tips
- Revise GCP & clinical trial lifecycle
- Understand eTMF & site processes
- Practice Clinical Quiz
📌 Tip: Strong knowledge of clinical workflow increases shortlist chances
🚀 Job Application Link
📌 Important Note Before You Apply:
Kindly read the full job description carefully before applying. Ensure your profile aligns with clinical trial coordination, tracking study milestones, clinical documentation management, ethics committee communications, and ICH-GCP regulatory compliance standards before proceeding.
Kindly read the full job description carefully before applying. Ensure your profile aligns with clinical trial coordination, tracking study milestones, clinical documentation management, ethics committee communications, and ICH-GCP regulatory compliance standards before proceeding.
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