Offer summary
Qualifications:
4-year college degree or equivalent, 3 to 4 years of TMF experience, 1 year as TMF Lead, Experience with Veeva Vault.Key responsabilities:
- Oversee and manage eTMF compliance
- Create and execute study TMF Plan
Precision for Medicine is hiring an experienced TMF Lead/Senior TMF lead to join our team, candidates can work remotely in Serbia, Poland, Hungary, Romania or Slovakia.
The TMF Lead/Senior TMF Lead is responsible for oversight, creation, management, and delivery of the eTMF in accordance with Good Clinical Practice (GCP), E6 ICH Guidelines and other regulatory guidance documents, relevant regulations (e.g., 21 CFR Parts 312 and 314, EMA Clinical Trials Directives), and Precision Standard Operating Procedures (SOPs) as appropriate. The Senior TMF Lead may take on responsibility for the complex and/or challenging studies. Additionally, the Senior TMF lead supports the development and implementation of TMF-related processes and systems.
Essential Functions of the job include but are not limited to:
· Creates and executes the study TMF Plan and project TMF Document Index. Ensures entire study team understands expectations, project-specific aspects of the TMF, and manages communication of any changes in the TMF.
· Attends and contributes to project kick-off meetings, project internal or external meetings, and ad hoc meetings as needed to ensure the project team is aware of the status of the eTMF, gaps, and escalations.
· Ensures the eTMF system is updated with the information related to countries, sites, contacts and applicable TMF document requirements.
· Engages and collaborates with the Project Manager and Functional Leads to ensure TMF documentation is submitted in a timely manner and with high quality to maintain the TMF in an inspection-ready state. Anticipates challenges to TMF compliance and identifies early signals of risk. Develops and implements plans to increase compliance and follows-up on non-compliance.
· Monitors and reports on TMF Health to internal team and sponsor. Identifies trends, risks, and overall status of the TMF.
· Serves as point of contact and Subject Matter Expert (SME) for project audits or inspections and supports in the report responses. Escalates to TMF management in cases of significant risk to Precision.
· Initiates and performs Quarterly Completeness/Compliance checks for assigned projects and ensures proper documentation.
· Identifies project team TMF training needs and provides or supports team re-education.
· Manages the close-out activities of assigned studies, including defining the timeline for final document submission, final document processing, close out of all outstanding queries, requesting the eTMF export from the vendor, transfers to the sponsor and collects the Acknowledgement of Receipt.
· Provides training and education to the Clinical Solutions functions to build knowledge and awareness of the good documentation practices and TMF on clinical trials.
· Manages projects within the Sponsor eTMF Systems and actively listens to deliver insightful solutions for challenges.
· Support process development or improvement initiatives within the Records Management department. Train and mentor junior Records Management team members for their TMF responsibilities
· Serves as a System Superuser and carrying out the activities assigned to them within tickets.
Qualifications:
Minimum Required:
Other Required:
Skills:
Competencies:
#LI-NC1 #LI-Remote
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Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC
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