tmf lead

DescriptionPosition Summary The TMF Lead is an independently resourceful subject matter expert (SME) responsible for the quality, completeness, and inspection readiness of Trial Master Files (TMFs) across assigned clinical studies, from study startup through study closeout and archive, within the Veeva TMF (Vault) system. Operating in a small biotech...

Mavericks Wanted  When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on   In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce...

Job DetailsNew ideas are all around us, but only a few will change the world. That’s our focus at JPL. We ask the biggest questions, then search the universe for answers—literally. We build upon ideas that have guided generations, then share our discoveries to inspire generations to come. Your mission—your opportunity—is to seek out the answers that...

Benefits:Dental insuranceHealth insuranceStock options planReports to: Reports to the VP, Clinical OperationsSPI is seeking a highly experienced and organized TMF Lead to support the operational execution of our clinical research programs.As a TMF Lead, you will lead the smooth execution of clinical trials from start-up to close-out, work closely with CRA(s)...

Overview Fortrea's FSP Team is hiring a TMF Lead II! Remote US. Seeking strong experience in heavy metrics reporting and KPI development. The TMF Management team is responsible for the completeness and accuracy of the Trial Master File (TMF) for all sponsored studies. The TMF Lead II is the Subject Matter Expert for TMF across all research phases and...

Benefits Dental insurance Health insurance Stock options plan Reports to: VP, Clinical Operations SPI is seeking a highly experienced and organized TMF Lead to support the operational execution of our clinical research programs. As a TMF Lead, you will lead the smooth execution of clinical trials from start‑up to close‑out, work closely with CRA(s) and...

BioCryst Pharmaceuticals, Inc. seeks a TMF Manager to lead and oversee TMF/eTMF strategies, ensuring high-quality, inspection-ready documentation across Phase I–IV studies.You will drive standardization of TMF/indexing, and collaborate with CRA, CROs, and IT on system configurations and training. Ideal candidates have 5+ years TMF/eTMF experience,...

BioCryst Pharmaceuticals, Inc. seeks a TMF Manager to lead and oversee TMF/eTMF strategies, ensuring high-quality, inspection-ready documentation across Phase I–IV studies.You will drive standardization of TMF/indexing, and collaborate with CRA, CROs, and IT on system configurations and training. Ideal candidates have 5+ years TMF/eTMF experience,...

Overview Fortrea's FSP Team is hiring a TMF Lead II! Remote US. Seeking strong experience in heavy metrics reporting and KPI development. The TMF Management team is responsible for the completeness and accuracy of the Trial Master File (TMF) for all sponsored studies. The TMF Lead II is the Subject Matter Expert for TMF across all research phases and...

We are currently hiring full-time office based individuals for an exciting career in clinical research managing our Trial Master File. The Trial Master File (TMF) is a collection of documentation that allows the conduct of a clinical trial, and the integrity of the data produced to be evaluated by Regulatory bodies, such as the FDA. The TMF is an important...

The TMF Senior Manager, Clinical Operations serves as the operational leader responsible for the strategy, governance, quality, and execution of the Trial Master File (TMF) across the clinical development portfolio. This role partners cross-functionally with Clinical Operations, Quality Assurance, Regulatory Affairs, Clinical Science, Biometrics, CROs, and...

BioCryst Pharmaceuticals is seeking a Trial Master File (TMF) Manager to develop, implement, and oversee TMF processes, systems, training, and archival of TMFs for Phase I–IV studies. You will serve as the TMF SME for eTMF and CTMS, ensuring inspection readiness and regulatory compliance across global trials.The role partners with study teams, CROs, and IT...

BioCryst Pharmaceuticals is seeking a Trial Master File (TMF) Manager to develop, implement, and oversee TMF processes, systems, training, and archival of TMFs for Phase I–IV studies. You will serve as the TMF SME for eTMF and CTMS, ensuring inspection readiness and regulatory compliance across global trials.The role partners with study teams, CROs, and IT...

Kymera Therapeutics is seeking an experienced professional to lead TMF management and drive compliance within clinical trials. The ideal candidate will have over 10 years in the biotech industry and a robust track record in TMF management, ensuring readiness for regulatory inspections.The role demands strong leadership, experience in strategic process...

Job descriptionWho We Are:TransPerfect is the world's largest provider of language services and technology solutions for global business. From offices in over 160 cities on six continents, TransPerfect offers a full range of services in 170+ languages to clients worldwide. More than 5,000 global organizations employ TransPerfect's GlobalLink® technology to...

COMPANY:At BioCryst, we share a deep commitment to improving the lives of people living with hereditary angioedema (HAE) and other rare diseases. We leverage our expertise in structure-guided drug design to develop first-in-class or best-in-class oral small-molecule and injectable protein therapeutics. Our global headquarters is in Durham, North Carolina, we...

A leading biopharmaceutical recruitment firm based in Cambridge is seeking a detail-oriented TMF Manager. This role ensures Trial Master Files (TMFs) are inspection-ready and comply with ICH GCP and GDP standards. Responsibilities include managing clinical documentation quality, overseeing eTMF systems, and leading vendor interactions. The ideal candidate...

Job OverviewProject Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs,...

The TMF Specialist is responsible for overseeing the overall management and quality of essential clinical trial documents to ensure compliance with applicable regulatory and local requirements. This position will provide management and oversight of Trial Master File (TMF) filing activities to ensure audit and inspection readiness for clinical...

Associate Director, Clinical Operations-TMF - (ADCOTMF_COMPANY_1.1) Job Title Associate Director, Clinical Operations-TMF Location Bethesda, MD 20817 US (Primary) Category Clinical Operations Job Type Full-Time Salary Range $130,000–$155,000/YR Education Master's Degree Travel None Job Description Owns Trial Master File (TMF) strategy,...