Das ist der Job
Manage TMF operations activities for multiple complex studies or sponsor portfolios.
Darum lohnt es sich
Work within a global and collaborative team environment. Exposure to international clinical research operations and industry best practices.
The company operates with a collaborative international team and values inclusion, professional growth, and purpose-driven healthcare work.
#J-18808-Ljbffr 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. Opportunity to contribute to clinical research projects that improve patients’ lives worldwide. Jobgether
This is a global clinical research environment focused on ensuring accuracy, compliance, and quality of essential trial documentation.
