TMF Lead
Clinical Careers Page(18 days ago)
About this role
A Trial Master File Lead at ICON supports clinical trial document management by overseeing TMF processes, ensuring compliance with regulations, and facilitating document quality and training. The role is home-based in Mexico and involves collaboration with various teams to maintain the integrity of trial records.
Required Skills
- TMF Management
- Regulatory Compliance
- Clinical Documentation
- Audit & Quality Checks
- Document Management
- Training and Support
- Project Coordination
- Healthcare Industry
- Clinical Trials
- Regulatory Standards
About Clinical Careers Page
iconplc.comICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.
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