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$122.21k - $144.4k
...various clinical, technical and business operations domains to strengthen our team of patient-centric, intelligent individuals. The TMF Operations Manager is responsible for owning and overseeing the management and quality control of Trial Master File (TMF) documentation...SuggestedFlexible hours$120k - $138k
...underway, we have an exciting opportunity to shape the future of cancer care and make a meaningful impact in the lives of patients. The TMF Document Specialist is responsible for owning and overseeing the management and quality control of Trial Master File (TMF)...SuggestedShift work- Marketing and Communications Specialist (TMF) Posted on July 24, 2018 Position Summary The Marketing and Communications Specialist is responsible for creating awareness and understanding of the Foundation as a “Giving Community” that builds relationships to build assets...SuggestedLocal area
$100k - $118k
Overview Fortrea's FSP Team is hiring a TMF Lead II! Remote US. Seeking strong experience in heavy metrics reporting and KPI development... ...and count, in collaboration with leads from each functional group within the study. Ensure ongoing "real-time" EDL maintenance updates...SuggestedFull timePart timeWork at officeRemote workFlexible hours$67.5k - $99k
A leading biopharmaceutical company in Cambridge, MA seeks a TMF Management Specialist. This role involves setting up and managing the Trial Master File, ensuring compliance with regulations, and overseeing financial documents related to clinical studies. Candidates should...Suggested- A leading biopharmaceutical company is seeking an experienced Associate Director for TMF oversight and inspection readiness. This role involves managing TMF integrity and compliance and leading inspection preparedness efforts. The ideal candidate will have substantial experience...Suggested
- A leading biopharmaceutical company in San Diego seeks a Senior Manager of Clinical Standards & Processes. In this critical role, you will oversee the eTMF process and ensure compliance with GCP and SOPs. The ideal candidate will have at least 8 years of experience in clinical...Suggested
- A global CRO is seeking a Trial Master File (TMF) Specialist for its Baltimore campus. The ideal candidate will manage the TMF, ensuring it is inspection-ready, support clinical trial execution, and collaborate closely with various teams. This position requires strong knowledge...SuggestedWork at office
$145.3k - $181.6k
...average. Position Summary The Associate Director, Trial Master File (TMF) Oversight & Inspection Readiness (IR) is responsible for leading... ...model; direct experience with the TMF Reference Model working group is preferred. Veeva Vault eTMF/CTMS experience preferred....SuggestedWork at officeLocal areaRemote workNight shift3 days per week- A leading healthcare company is seeking an Associate Director, Trial Master File Oversight & Inspection Readiness. You will manage TMF governance and inspection readiness, ensuring compliance with regulations. The ideal candidate has a Bachelor's degree in life sciences...Suggested
$67.3k - $71.13k
Program and Grants Associate, Grants & Information Management (TMF) Posted on March 16, 2020 The McKnight Foundation seeks a professional... .... Ability to communicate effectively interpersonally and in group settings. Ability to constructively navigate differences to arrive...SuggestedFull timeWork experience placementWork at officeFlexible hours- ...Operations Specialist Contractor to enhance clinical trial efficiency. This position focuses on the management of clinical trial systems and TMF activities, ensuring compliance with regulatory requirements. Candidates should have 5+ years in clinical operations and expertise...SuggestedRemote jobFor contractorsWork at office
- ...company is seeking an Associate Director for Trial Master File Oversight & Inspection Readiness. This role will lead the oversight of TMF processes and ensure compliance with regulatory standards, safeguarding the organization during inspections. Candidates should have...Suggested
- A leading biotech company in Massachusetts is seeking a highly motivated college student for a co-op position in Risk Management and Compliance. This role offers firsthand experience in assisting with continuous improvement initiatives, GCP oversight, and support for clinical...SuggestedFull time
- ...The successful candidate will manage clinical trial systems, ensuring compliance with regulatory standards while providing support for TMF management. With a focus on optimization of clinical operations processes, this role requires strong problem-solving skills and at...SuggestedRemote jobFor contractors
$65k - $80k
Trial Master File (TMF) Specialist - Clinical Trials Location: Pharmaron Baltimore Campus, Baltimore Compensation: $65-80K Annually About Pharmaron Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech companies bring new therapies to life...Full timeContract workTemporary workWork at officeWorldwideWork visaFlexible hours$20 - $60 per hour
**The Role:**Moderna’s Development Clinical Risk, Compliance, TMF & Systems (RCTS) group is seeking a highly motivated college student that has an interest in Risk Management and Compliance in the RCTS environment within the biotech/pharma industry. This position provides...Full timeWork at officeRelocationShift work- A prominent nonprofit organization in Savannah, GA is seeking a TMF Specialist to manage clinical trial documents ensuring compliance and readiness for audits. This role involves overseeing TMF filing, supporting clinical teams, and conducting quality reviews. The ideal...
- ...an Associate Director for Trial Master File Oversight & Inspection Readiness. This role will lead the operational oversight for the TMF, ensuring integrity, regulatory compliance, and inspection preparedness within Clinical Operations. Candidates should possess a Bachelor...Work at office3 days per week
- ...pharmaceutical company is seeking an Associate Director for Trial Master File Oversight & Inspection Readiness. This role involves leading TMF operational oversight to ensure integrity and compliance, while maintaining inspection readiness. Candidates should possess a...
- A progressive oncology firm is seeking a TMF Document Specialist to oversee management and quality control of TMF documentation across global studies. This essential role requires at least 5 years of experience in TMF Operations, ensuring compliance with regulatory standards...
- A biotechnology company in New Haven, CT, is offering a summer internship in Clinical Operations. This position will support activities such as assisting with study documentation and trial master file maintenance, and tracking study timelines. Ideal candidates are current...InternshipSummer internshipRemote work
- A healthcare staffing agency is seeking a Clinical Trial Assistant for a hybrid role in California. This entry-level position offers an opportunity to support clinical trials through administrative duties. Responsibilities include managing trial documentation, coordinating...
$145.3k - $181.6k
...Trial Master File oversight. This role requires at least 8 years of experience in the pharmaceutical industry, with a strong emphasis on TMF integrity and inspection readiness. The ideal candidate will lead cross-functional teams and ensure compliance with regulatory...- ...and oversight of Trial Master File operations. This remote or hybrid role (if based in CA) will involve developing standards, managing TMF-related vendors, and ensuring compliance with regulations. Candidates should possess a relevant bachelor's degree and have over 8...Remote job
$140k - $180k
...focused on developing transformative oncology therapies. As we advance our clinical pipeline, we are seeking an Associate Director, TMF Operations to lead Trial Master File (TMF) operations across our oncology programs. This role provides strategic leadership and oversight...Full time3 days per week- ...new therapies to patients in need. The Position The Senior Manager of Clinical Standards & Processes (CS&P) will act as the internal TMF lead on all studies, ensuring oversight to outsourced TMF work (vendor and/or CRO) and performing oversight to TMF metrics and trends...
- A leading clinical research organization is seeking a Senior Clinical Trial Associate to act as a central contact for clinical study teams. This role involves managing trial documents, coordinating with regulatory affairs, and ensuring timelines are met. Candidates should...
$100k - $118k
A clinical research organization is looking for a TMF Lead II to oversee Trial Master File management across all studies. This role involves heavy metrics reporting, supports compliance with ICH/GCP guidelines, and requires a minimum of 7 years of clinical research experience...Remote job- A leading clinical research organization is seeking a TMF Lead II to manage and support the Trial Master File. The role involves overseeing TMF completeness and compliance, driving inspection readiness, and managing project metrics. Ideal candidates should have a BS/BA...Remote job