TMF Coordinator for Clinical Trials
Save this job and keep your search organized
Create a free account to save jobs, create alerts and return to this listing from your dashboard.
By continuing, you agree to our Terms & Privacy Policy.
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 opportunity 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
- 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