Darum lohnt es sich
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.
• 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. • 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.
Jobgether
This is a global clinical research environment focused on ensuring accuracy, compliance, and quality of essential trial documentation.
