TMF/eTMF & ISF Management jobs

FSP Clinical Trial Coordinator - Site Record Coordination

Thermo Fisher Scientific · Posted Nov 12, 2026

Open

Bangalore, India
On-site
1–3 years

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FSP Clinical Trial Coordinator - Site Record Coordination

Thermo Fisher Scientific · Posted Nov 12, 2026

Open

Bangalore, India
On-site
1–3 years

Apply with Referso

FSP Clinical Trial Coordinator - Site Record Coordination

Thermo Fisher Scientific · Posted Nov 12, 2026

Open

Hyderabad, Telangana, India
Associate
1–3 years

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The Clinical Trial Coordinator I supports clinical trial operations by managing site documentation, TMF/eTMF activities, clinical systems, site communications, and study records to ensure timely, compliant, and high-quality trial execution.

Responsibilities

Plan, distribute, collect, and track site records through Site Collaboration tools and ensure timely TMF completion.
Perform quality reviews of study documentation and maintain TMF/eTMF, ISF, and study records.
Support clinical systems including CTMS, Activate, and eTMF, ensuring databases and trackers remain current.
Coordinate with sites and internal teams for document collection, site start-up, feasibility, and regulatory activities.
Review study metrics, resolve documentation findings, and communicate site-related risks and updates.

Requirements

Bachelor's degree preferred in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related discipline
Nice to have: Veeva

Skills

Clinical Trial Operations TMF/eTMF & ISF Management CTMS and Clinical Trial Systems Site Collaboration & Site Documentation

FSP Clinical Trial Coordinator - Site Record Coordination

Thermo Fisher Scientific · Posted Nov 12, 2026

Open

Mumbai, Maharashtra, India
Associate
1–3 years

Apply with RefersoAI Apply on careers page

Responsibilities

Plan, distribute, collect, and track site records through Site Collaboration tools and ensure timely TMF completion.
Perform quality reviews of study documentation and maintain TMF/eTMF, ISF, and study records.
Support clinical systems including CTMS, Activate, and eTMF, ensuring databases and trackers remain current.
Coordinate with sites and internal teams for document collection, site start-up, feasibility, and regulatory activities.
Review study metrics, resolve documentation findings, and communicate site-related risks and updates.

Requirements

Bachelor's degree preferred in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related discipline
Nice to have: Veeva

Skills

Clinical Trial Operations TMF/eTMF & ISF Management CTMS and Clinical Trial Systems Site Collaboration & Site Documentation