Study Tracking & Reporting jobs

FSP Prin Clinical Trial Coordinator

Thermo Fisher Scientific · Posted Nov 12, 2026

Open

Hyderabad, Telangana, India
Senior
6+ years

Apply with Referso

FSP Prin Clinical Trial Coordinator

Thermo Fisher Scientific · Posted Nov 12, 2026

Open

Hyderabad, Telangana, India
Senior
6+ years

Apply with Referso

FSP Prin Clinical Trial Coordinator

Thermo Fisher Scientific · Posted Nov 12, 2026

Open

Mumbai, Maharashtra, India
Senior
6+ years

Apply with RefersoAI Apply on careers page

Responsible for coordinating and supporting end-to-end clinical trial activities, ensuring operational excellence, regulatory compliance, and timely study execution.

Responsibilities

Coordinate and track study activities, timelines, and deliverables
Maintain and review eTMF/TMF, CTMS, study trackers, and trial documentation
Support regulatory submissions, audit readiness, and compliance with ICH-GCP and SOPs
Schedule meetings, prepare meeting minutes, and facilitate communication across study teams
Manage study supplies, investigator files, vendor trackers, and trial systems

Requirements

Bachelor's degree preferred (Life Sciences, Pharmacy, Clinical Research, or related field)
Nice to have: Veeva Vault

Skills

Clinical Trial Operations CTMS & eTMF/TMF Management Regulatory Documentation & ICH-GCP Meeting Coordination & Minutes of Meetings Study Tracking & Reporting

FSP Prin Clinical Trial Coordinator

Thermo Fisher Scientific · Posted Nov 12, 2026

Open

Bangalore, India
6+ years

Apply with RefersoAI Apply on careers page

Responsible for coordinating and supporting end-to-end clinical trial activities, ensuring operational excellence, regulatory compliance, and timely study execution.

Responsibilities

Coordinate and track study activities, timelines, and deliverables
Maintain and review eTMF/TMF, CTMS, study trackers, and trial documentation
Support regulatory submissions, audit readiness, and compliance with ICH-GCP and SOPs
Schedule meetings, prepare meeting minutes, and facilitate communication across study teams
Manage study supplies, investigator files, vendor trackers, and trial systems

Requirements

Bachelor's degree preferred (Life Sciences, Pharmacy, Clinical Research, or related field)

Skills

Clinical Trial Operations CTMS & eTMF/TMF Management Regulatory Documentation & ICH-GCP Meeting Coordination & Minutes of Meetings Veeva Vault (preferred)Study Tracking & Reporting