Trial Master File Specialist at SciPro in San Francisco, California

Posted in Other about 4 hours ago.

Type: full-time





Job Description:

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 Education
  • Bachelor's degree, ideally in biological sciences or a health-related field
  • At least 2 years of TMF management experience within Pharmacovigilance/Safety
  • Strong understanding of international safety regulations and compliance in safety reporting
  • Proficient in the DIA TMF Reference Model or equivalent, ICH-GCP, ALCOA+ standards, and document management regulations
  • Demonstrated ability to manage TMFs effectively, including developing related processes and policies
  • Ability to work well in collaborative, fast-paced team settings, adapting as needed
  • Excellent communication, interpersonal, and decision-making skills
  • Strong commitment to prioritizing tasks and achieving deliverables with high standards
  • 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 plus
  • Willingness to travel up to 25%, if working remotely

Pay rate: $35 - $40/hr. W2

Preferred Skills, Experience and Education
  • Experience working with CROs/vendors and management of external resources
  • Oncology experience, early and/or late stage

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