Looking to start your career in clinical research? A Clinical Trial Coordinator I (FSP) role is now open for candidates in Mumbai (fully remote). This entry-level opportunity is ideal for life sciences graduates seeking hands-on exposure in clinical trial operations, site activation, and regulatory support within a global CRO environment.
With involvement in over 2,700 clinical trials across 100+ countries, this organization offers unmatched exposure to global drug development processes, making it a strong launchpad for freshers and early-career professionals.
Key Responsibilities – Clinical Trial Coordinator I
As a Clinical Trial Coordinator, you will support project teams in executing clinical trials efficiently:
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- Coordinate and manage assigned clinical trial activities as per task matrix
- Perform eTMF (electronic Trial Master File) and investigator file reviews
- Support site activation and regulatory submissions
- Maintain and update clinical trial systems like Activate and CTMS
- Process, track, and upload study documents to client systems
- Assist in site feasibility, site selection, and site tiering processes
- Prepare and distribute Investigator Site Files (ISF) and study materials
- Analyze study metrics and resolve documentation discrepancies
- Support audit readiness and ensure compliance with ICH-GCP guidelines
- Coordinate with internal teams, sponsors, and investigator sites
- Maintain vendor trackers and regulatory documentation
- Participate in training and onboarding of new staff (if required)
Eligibility Criteria & Qualifications
Education:
- Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field (preferred)
- Diploma or equivalent qualification with relevant training also considered
Experience:
- 0–1 year experience (Freshers can apply)
Required Skills for Clinical Trial Coordinator Role
- Strong understanding of clinical research processes and SOPs
- Knowledge of ICH-GCP guidelines and regulatory requirements
- Excellent organizational and multitasking abilities
- Proficiency in MS Office (Excel, Word, PowerPoint)
- Strong communication and documentation skills
- Ability to manage timelines, risks, and priorities effectively
- Detail-oriented with analytical thinking capability
Why Apply for This Role?
- ✅ Fully Remote Job – Work from home flexibility
- ✅ Entry-level opportunity in clinical research industry
- ✅ Exposure to global clinical trials and top pharma companies
- ✅ Strong career growth in clinical operations & project management
- ✅ Opportunity to work with experienced professionals in a structured environment
How to Apply
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