TMF Specialist

Responsibilities: Responsible for day-to-day system administration and overall system maintenance. Responsible for training all users of the eTMF and ensuring the training program is kept up to date with system and procedure training. Responsible for overall quality, maintenance, and completeness of Trial Master Files. Identify trends or quality concerns and oversee the resolution of any issues. Work closely with Information Technology to ensure system validation is maintained. Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory requirements. Act as a liaison between the Site IRBs and Clinical team to resolve queries and concerns. Prepare and assist in the submission of protocol amendments, IND safety reports, consent form changes, and continuing reviews. Perform investigation of deviations and monitoring of Corrective actions & preventive actions (CAPA) relating to non-compliance issues and findings. Oversee TMF maintenance done by CROs and ensure final transfer of TMF is sufficient to support any potential regulatory filings. Other duties as assigned.

Qualifications: Bachelor's degree or higher in life sciences, health sciences, nursing, pharmacy, or related field. A minimum of 1 year of clinical research experience in academic and/or industry settings Prior eTMF/Veeva administration required. Demonstrate a comprehensive knowledge of Good Clinical Practice, Good Documentation Practice, and International Council for Harmonization E6(R2). Knowledge of, and direct experience with Trial Master Files, experience with electronic TMF systems is required. Fundamental knowledge of the conduct of clinical trials is preferred. Strong focus on teamwork, attention to detail, excellent organizational skills. Must have the ability to prioritize, and the ability to work in a multi-task environment. Must be able to work independently and professionally.