Thermo Fisher Scientific FSP Clinical Trial Coordinator Job – Mumbai, India

Thermo Fisher Scientific is hiring for the position of FSP Clinical Trial Coordinator – eTMF in Mumbai, India. Candidates with a Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology or Clinical Research and 1–3 years of experience can apply. This Clinical Trial Coordinator Job is open to candidates with relevant qualifications and experience.

Clinical Trial Coordinator Job Details

Job Title: FSP Clinical Trial Coordinator – eTMF

Company: Thermo Fisher Scientific

Location: Mumbai, India (Fully Remote)

Job Type: Full time, Standard (Mon–Fri)

Job Requisition ID: R-01375034

Role Summary

In this Clinical Trial Coordinator Job, the Clinical Trial Coordinator I supports the planning, execution and administration of clinical trials by managing trial documentation, clinical systems, site activities, regulatory processes and study tracking, working with study teams, investigators and internal stakeholders.

Key Responsibilities

  • Maintain and manage TMF/eTMF and ISF documentation, ensuring completeness and audit readiness.

  • Support study setup and execution by coordinating trial materials, site documentation and regulatory submissions.

  • Manage clinical systems (CTMS, Activate, eTMF), study trackers, reports and access management.

  • Support site qualification, feasibility, site start-up and investigator documentation activities.

  • Coordinate study supplies, vendor interactions, logistics and site communications.

  • Review study metrics, maintain databases and complete assigned tasks on time.

  • Collaborate with cross-functional teams to ensure compliance with ICH-GCP, SOPs and regulatory requirements.

Education & Experience

  • Bachelor’s degree preferred in Life Sciences, Pharmacy, Biotechnology, Clinical Research or a related field.

  • 1–3 years of experience in Clinical Research, Clinical Operations or Trial Coordination.

  • Understanding of ICH-GCP, clinical trial processes and regulatory requirements preferred.

  • Hands-on experience in global clinical trials and eTMF systems (preferably Veeva).

  • Experience taking minutes of study call meetings.

Required Skills

  • Clinical trial coordination and clinical operations

  • eTMF/TMF and ISF management; CTMS, Activate and clinical systems

  • Regulatory documentation and site start-up support

  • Feasibility and site qualification activities

  • MS Office (Excel, Word, PowerPoint, Outlook)

  • Strong communication, organization and documentation skills

How to Apply

Interested candidates can apply online through the official Thermo Fisher careers page for this Clinical Trial Coordinator Job.

CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE