Senior TMF Specialist
Clinical Careers Page(21 days ago)
About this role
ICON plc is seeking a Senior TMF Specialist to manage the Trial Master File for clinical trials, ensuring regulatory compliance and efficiency in documentation processes. The role involves performing completeness checks, collaborating with study teams, and maintaining inspection readiness.
Required Skills
- Veeva Vault
- eTMF
- Document Management
- Regulatory Compliance
- Clinical Trials
- Metadata Check
- Communication
- Organizational Skills
- Excel
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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