Join our TMF Operations team as a TMF Coordinator focused on ensuring quality and compliance in Trial Master File documentation. This role supports clinical trials through effective document management and collaboration. We're seeking a detail-oriented TMF Coordinator to manage TMF documentation adhering to global regulations.
Your responsibilities will include maintaining a comprehensive TMF structure, ensuring inspection readiness, and enhancing collaboration with cross-functional teams. This position offers the prospect to contribute to essential clinical trial management. Key Responsibilities:
- Maintain TMF structures and ensure compliance with regulations
- Support inspection readiness and audit activities effectively
- Accurately file and manage TMF documents within our systems
- Perform quality control checks on TMF documents
- Collaborate with study teams to ensure documentation is complete Requirements:
- Bachelor’s degree in Life Sciences or related field
- 1-3 years of TMF management experience
- Knowledge of eTMF platforms and regulations
- Strong attention to detail and organizational skills
- Ability to work remotely and manage multiple tasks Bring your expertise in TMF management and compliance to drive clinical trial success.