Thermo Fisher Scientific is hiring experienced professionals for the position of Clinical Trial Coordinator (FSP) in India. This is a fully remote opportunity based in Mumbai, offering candidates the chance to work on global Phase II and Phase III clinical trials while supporting leading pharmaceutical companies and biotechnology organizations.
The Clinical Trial Coordinator role is ideal for professionals with experience in global clinical operations, Veeva Vault eTMF, CTMS, site activation, TMF management, and regulatory inspection readiness. If you have 2+ years of clinical trial coordination experience and want to work in a global clinical research environment, this opportunity offers excellent career growth.
Job Details
- Position: Clinical Trial Coordinator (FSP)
- Company: Thermo Fisher Scientific
- Job Type: Full-Time
- Work Mode: Fully Remote
- Location: Mumbai, Maharashtra, India
- Experience: 2+ Years
- Department: Clinical Operations
- Industry: Clinical Research / CRO
Key Responsibilities
- Support day-to-day clinical trial operations for global studies.
- Assist Clinical Operations Managers and Study Managers throughout the study lifecycle.
- Review essential study documents including informed consent forms, study plans, and regulatory packets.
- Support site activation activities and develop critical activation timelines.
- Maintain inspection readiness and ensure compliance with SOPs and ICH-GCP guidelines.
- Support CTMS and Veeva Vault eTMF activities.
- Participate in study meetings and prepare meeting minutes.
- Coordinate vendor contract administration.
- Assist with financial reconciliation during study close-out.
- Support risk-based monitoring activities.
- Maintain trial documentation and regulatory compliance.
- Assist onboarding and training of new team members when required.
Required Qualifications
- Bachelor’s Degree in Life Sciences, Pharmacy, Biotechnology, Nursing, or related discipline.
- Minimum 2 years of Clinical Trial Coordinator, Clinical Trial Associate, or Project Coordinator experience.
- Experience supporting global clinical trials.
- Hands-on experience with Veeva Vault eTMF lifecycle.
- Experience with CTMS and clinical trial documentation.
- Knowledge of ICH-GCP guidelines and country regulations.
- Excellent communication and organizational skills.
- Strong Microsoft Office skills (Excel, Word, PowerPoint).
- Ability to work independently in a remote environment.
Preferred Skills
- Phase II and Phase III clinical trial experience.
- Oncology study experience.
- Global or international clinical trial exposure.
- Risk-based monitoring support.
- Site activation expertise.
- Vendor coordination.
- Regulatory inspection readiness.
- Documentation management.
- Clinical project coordination.
Why Join Thermo Fisher Scientific?
- Fully Remote Work Opportunity
- Exposure to Global Clinical Trials
- Work with Top Pharmaceutical Sponsors
- International Project Experience
- Career Growth in Clinical Operations
- Professional Learning & Development
- Collaborative Global Teams
- Competitive Salary & Benefits
Salary
Expected Salary: โน8,00,000 โ โน14,00,000 per annum (CTC), depending on experience and qualifications.
How to Apply
