TMF Specialist
Job in
Bethesda, Montgomery County, Maryland, 20811, USA
Listed on 2026-10-05
Listing for:
Zachary Piper Solutions
Full Time
position Listed on 2026-10-05
Job specializations:
-
Pharmaceutical
Regulatory Compliance Specialist, Healthcare Compliance
Job Description & How to Apply Below
Piper Companies is looking for a TMF Specialist to join a clinical research organization located in Bethesda, MD
.
- Managing TMF set-up, quality oversight, reporting, metrics, and quality control activities
- Maintaining overall TMF document quality and completeness, including proper filing, coordination, tracking, and reporting
- Ensuring clinical trial documentation complies with eTMF specifications, ICH/GCP guidelines, regulatory requirements, and internal SOPs
- Accurately maintaining all TMF records in accordance with SOPs and data standards to support inspection readiness
- Responding to client requests for TMF retrieval, reproduction, re-filing, and delivery of electronic records
- Supporting the development and maintenance of TMF training materials, SOPs, and guidelines, including training staff as needed
- Assisting with audit and inspection readiness activities and ensuring the TMF remains inspection ready
- Staying current on TMF Reference Model standards, regulatory requirements, and industry best practices
- Serving as a liaison between eTMF records management and internal and external clients
- Monitoring project activities to ensure deadlines and deliverables are met
- Acting as a subject matter expert on TMF-related matters and providing guidance to project staff and subcontractors
- Performing quality control reviews of TMF documents to ensure accuracy
- Coordinating retrieval of requested records and preparing closed studies for transfer within agreed timelines
- Assisting management with records management planning, cost proposals, and resource forecasting
- Performing task management and, depending on experience level, line management responsibilities
- Experience working with eTMF systems;
Veeva Vault or Trial Interactive preferred - Strong understanding of clinical research processes and document management requirements
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements related to TMF management
- Excellent organizational skills with strong attention to detail
- Effective written and verbal communication skills
- Ability to manage multiple priorities in a fast-paced, deadline-driven environment
- Strong problem-solving and analytical skills
- Experience advising project teams on TMF-related issues
- Experience training, mentoring, and coaching staff
- Ability to build and maintain positive working relationships across teams and management
- Proficiency in Microsoft Office
- Bachelor's degree in a science or healthcare-related field required
- Rate Range: $20-35/hr
- Comprehensive Benefit Package:
Cigna Medical/Dental/Vision, 401K, Sick Leave as Required by Law
This job is open for applications on September 22nd, 2026. Applications will be accepted for at least 30 days from the posting date.
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