TMF Specialist I
Clinical Careers Page(1 month ago)
About this role
ICON plc is a global healthcare intelligence and clinical research organization. The TMF Specialist I is an entry-level role supporting the integrity and administration of Trial Master File processes to meet client and company standards. The position sits within clinical research operations and contributes to maintaining compliance and documentation quality across studies.
Required Skills
- TMF
- Document Management
- Compliance
- Organization
- Collaboration
- Communication
- Detail Oriented
- Clinical Research
Qualifications
- Bachelor's Degree
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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