Manage TMF operations activities for multiple complex studies or sponsor portfolios.
Oversee Trial Master File quality control processes, including planning, tracking, reporting, and follow-up on compliance issues.
Support regulatory inspections, sponsor audits, and resolution of audit findings when required.

Requirements:

University degree preferred, ideally in Life Sciences or a related field.
2-4 years of relevant experience in a highly regulated industry, CRO, pharmaceutical, or clinical research environment.
Strong understanding of clinical research principles, industry standards, and TMF management requirements.

Benefits:

Opportunity to contribute to clinical research projects that improve patients’ lives worldwide.
Work within a global and collaborative team environment.
Exposure to international clinical research operations and industry best practices.

Jobgether

This is a global clinical research environment focused on ensuring accuracy, compliance, and quality of essential trial documentation. The company operates with a collaborative international team and values inclusion, professional growth, and purpose-driven healthcare work.

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