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Hiring Clinical Trial Coordinator I
🏢 Thermo Fisher Scientific
📍 Mumbai / Remote
⏳ Freshers
💻 Clinical Research
Start your career in clinical research & clinical trials with Thermo Fisher Scientific. This Clinical Trial Coordinator I role offers hands-on experience in trial operations, documentation, and global studies — perfect for freshers.
📋 Job Overview
- Role: Clinical Trial Coordinator I (FSP)
- Location: Mumbai / Remote
- Experience: Freshers / 0–1 year
- Industry: Clinical Research
- Work Mode: Remote
📌 Key Responsibilities
- Support clinical trial operations & coordination
- Maintain eTMF & regulatory documents
- Assist in site activation & submissions
- Update CTMS & trial systems
- Handle study documentation & tracking
- Ensure ICH-GCP compliance
- Support audit readiness & reporting
🎓 Eligibility
- B.Pharm / M.Pharm / PharmD / BSc / MSc / Life Sciences
- Freshers can apply
- Basic knowledge of clinical trials preferred
💻 Required Skills
- Knowledge of clinical research & GCP
- Documentation & coordination skills
- MS Excel, Word, PowerPoint
- Communication & multitasking
🚀 Career Growth
- Clinical Trial Coordinator → CRA → Project Manager
- Clinical Research Career Guide
💡 Interview Tips
- Revise ICH-GCP basics
- Understand clinical trial workflow
- CTA Practice Quiz
- Aptitude Practice
📄 Resume Tips
- Add internships or clinical exposure
- Highlight GCP & documentation knowledge
- Use keywords: eTMF, CTMS, Clinical Trials
- Career Guide
📌 Tip: Remote + fresher role — high competition. Apply early.
🚀 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, study site management support, tracking trial milestones, maintenance of clinical trial documentation (TMF), and ICH-GCP regulatory guidelines compliance before proceeding.
Kindly read the full job description carefully before applying. Ensure your profile aligns with clinical trial coordination, study site management support, tracking trial milestones, maintenance of clinical trial documentation (TMF), and ICH-GCP regulatory guidelines compliance before proceeding.
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