Thermo Fisher Clinical Trial Coordinator I (Remote, Mumbai)
Thermo Fisher Scientific is hiring for 2 Clinical Trial Coordinator I positions in Mumbai under its Functional Service Provider clinical operations team. These Clinical Trial Coordinator Jobs are open to candidates with a Bachelor’s degree in Life Sciences and 1–3 years of experience.
Job Details
Company: Thermo Fisher Scientific
Job Role: Clinical Trial Coordinator I
Total Openings: 2 Positions
Job Type: Full Time
Work Mode: Fully Remote
Work Schedule: Monday to Friday
Experience: 1–3 Years
Qualification: Bachelor’s Degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research or related field
Industry: Clinical Research
Locations: Mumbai & Bangalore
Clinical Trial Coordinator Jobs: Key Responsibilities
FSP Clinical Trial Coordinator – Site Record Coordination (Mumbai):
- In this Clinical Trial Coordinator role, plan, distribute, collect, and track site records using Site Collaboration tools.
- Perform quality reviews of study documentation and maintain TMF/eTMF and ISF records.
- Support CTMS, Activate, and eTMF systems.
- Coordinate with clinical sites and internal teams for document collection, site start-up, feasibility, and regulatory activities.
- Review study metrics and resolve documentation findings.
- Communicate site-related risks and study updates.
- Support vendor management, regulatory submissions, and site communications.
- Ensure compliance with ICH-GCP, SOPs, and Good Documentation Practices.
FSP Clinical Trial Coordinator – eTMF (Bangalore):
- Maintain TMF/eTMF and ISF documentation, ensuring completeness and audit readiness.
- Support study setup, trial materials, site documentation, and regulatory submissions.
- Manage CTMS, Activate, and eTMF systems, study trackers, reports, and access management.
- Support site qualification, feasibility, site start-up, and investigator documentation.
- Coordinate study supplies, vendor interactions, logistics, and site communications.
- Review study metrics and maintain study databases.
- Collaborate with cross-functional teams to ensure compliance with ICH-GCP, SOPs, and regulatory requirements.
Eligibility Criteria
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or a related discipline.
- 1–3 years of experience in Clinical Research, Clinical Operations, TMF/eTMF, Clinical Trial Coordination, or trial support functions.
- Hands-on experience working on global clinical trials.
- Experience using eTMF systems, preferably Veeva.
- Understanding of ICH-GCP, clinical trial processes, and regulatory requirements.
- For the Site Record Coordination position, experience managing site-related files and collaborations with European and US sites is preferred.
Required Skills
- Clinical Trial Operations
- Clinical Trial Coordination
- TMF/eTMF and ISF Management
- CTMS and Activate
- Veeva eTMF
- Site Collaboration and Documentation
- Regulatory Documentation
- Site Start-up and Feasibility
- ICH-GCP and Good Documentation Practices
- Clinical Systems and Study Tracking
- Vendor and Stakeholder Coordination
- Microsoft Office Suite
- Communication and Organizational Skills
How to Apply
Apply via the employer’s official career page: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE