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...

Zohorecruit seeks a TMF Manager to lead a team of TMF professionals in an office-based setting. You will drive TMF strategy, ensure high-quality documentation, and collaborate with trial teams to support regulatory readiness including audits and inspections.Reporting to senior leadership, you will oversee TMF processes across studies, ensuring consistency...

Arcus Biosciences is seeking a Senior Clinical Document Specialist to manage TMF documents across trials, ensuring GCP and 21 CFR compliance and eTMF accuracy. The role involves close collaboration with Study Management Teams and TMF owners, performing QC, classification, and reconciliation of essential documents and supporting transfer activities from...

Arcus Biosciences is seeking a Senior Clinical Document Specialist to manage TMF documents across trials, ensuring GCP and 21 CFR compliance and eTMF accuracy. The role involves close collaboration with Study Management Teams and TMF owners, performing QC, classification, and reconciliation of essential documents and supporting transfer activities from...

Job Description Job Description Benefits: Dental insurance Health insurance Stock options plan Reports to: Reports to the 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...

Job Description Job Description Benefits: Dental insurance Health insurance Stock options plan Reports to: Reports to the 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...

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...

Industry Nonprofit Charitable OrganizationsWork Experience 1-3 yearsCity AuburnState/Province MaineCountry United StatesJob DescriptionWe 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...

The Role: The Manager, TMF Systems and Operations plays a key role in supporting the daily operations and maintenance of Moderna’s Clinical Trial Management System (CTMS), eTMF system and Trial Master File (TMF). This role ensures study systems are properly configured, maintained, and compliant with regulatory and company standards.The Manager partners...

Madrigal Pharmaceuticals is seeking an Associate Director of TMF Operations to lead day-to-day TMF strategy, oversight, and inspection readiness across studies. You will manage FSP resources, ensure QA oversight, and drive metrics-driven governance with cross-functional teams.The role requires strong TMF expertise, vendor oversight capability, and experience...

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organization, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.Check...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Sr. TMF Specialist - Contract based in United States. This is a senior-level Clinical Operations opportunity focused on maintaining the operational integrity, quality, and organization of the Trial Master File (TMF). You will...

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...

TMF Senior Manager, Clinical Operations 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...

Position Overview We are seeking an experienced Associate Director, Clinical Operations (TMF) to provide strategic and operational leadership for Trial Master File (TMF) management across a portfolio of clinical programs at a global contract research organization (CRO). This individual will be responsible for TMF strategy, inspection readiness, quality...

Position Summary: Biomea Fusion is hiring a Sr. TMF Specialist, who will be responsible for maintaining the operational aspects of the TMF system and supporting TMF-related activities.  This is a contract position for approximately 6 months.   Essential Responsibilities: Uploading documents into the TMF Performing QC of the documents in the...

Alfasigma is a privately held global healthcare company founded over 75 years ago in Italy, where it remains headquartered today in Bologna and Milan. The Group operates in over 100 markets spanning Europe, North and South America, Asia, and Africa. Over three years ago, we embarked on a transformative journey to become a truly global innovative healthcare...

Senior Clinical Document Specialist This position is responsible for collecting, reviewing, maintaining, and archiving essential Regulatory documents for the Trial Master File (TMF) 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...

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...

Description This position is responsible for collecting, reviewing, maintaining, and archiving essential Regulatory documents for the Trial Master File (TMF) 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...