Trial Master File (TMF) Specialist
6-month initial contract (potential for extension & possible conversion to FTE)
San Francisco Bay Area, CA (hybrid)
Responsibilities
- :Act as the primary GPS TMF lead, coordinating cross-functional TMF management for clinical studies
- .Follow Standard Operating Procedures (SOP), Good Clinical Practice (GCP), International Conference on Harmonization (ICH) guidelines, and ALCOA+ standards
- .Update cross-functional teams on TMF filing progress to support study objectives
- .As the GPS subject matter expert, draft, review, and oversee all eTMF Plans, Index, SOPs, and related documents
- .Perform quality checks on uploaded documents to ensure accuracy and correct indexing
- .Oversee the quality of study TMFs, managing TMF metrics and key performance indicators (KPIs)
- .Collaborate with CROs/vendors and team members to coordinate TMF activities
- .Manage systems for cataloging, filing, retrieving, saving, and transferring TMF records for both internal and vendor processes
- .Build and maintain effective working relationships with CROs/vendors for TMF management
- .Support GPS TMF-related audit and inspection activities
- .Contribute to eTMF uploads for applicable clinical studies, as needed
- .Engage in other GPS functions as appropriate
.
Required Skills, Experience, and Educatio
- n:Bachelor’s degree, ideally in biological sciences or a health-related fiel
- d.At least 2 years of TMF management experience within Pharmacovigilance/Safet
- y.Strong understanding of international safety regulations and compliance in safety reportin
- g.Proficient in the DIA TMF Reference Model or equivalent, ICH-GCP, ALCOA+ standards, and document management regulation
- s.Demonstrated ability to manage TMFs effectively, including developing related processes and policie
- s.Ability to work well in collaborative, fast-paced team settings, adapting as neede
- d.Excellent communication, interpersonal, and decision-making skill
- s.Strong commitment to prioritizing tasks and achieving deliverables with high standard
- s.Proficient in SharePoint and various eTMF platforms (e.g., Veeva, Trial Interactive, WingSpan, FLEX
- ).Skilled in Microsoft Office (Outlook, Word, Excel, PowerPoint); knowledge of MS Project or Smartsheet is a plu
- s.Willingness to travel up to 25%, if working remotel
y.
Pay rate: $35 - $40/hr.
W2
Preferred Skills, Experience and Educat
- ion:Experience working with CROs/vendors and management of external resou
- rcesOncology experience, early and/or late s
tage