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- ...Charitable Organizations Work Experience 1-3 years City Cumberland State/Province Maryland Country United States Job Description The TMF Specialist is responsible for overseeing the overall management and quality of essential clinical trial documents to ensure compliance...SuggestedWork experience placementWork at officeLocal areaFlexible hours
$35 - $45 per hour
...intended to evaluate ivonescimab in combination with chemotherapy compared with bevacizumab plus chemotherapy. Overview of Role The TMF Associate supports the day-to-day operational management of the Trial Master File (TMF) within Veeva Vault eTMF. This role is responsible...SuggestedWork at office- ...Hybrid — New York City Step into a role where precision meets purpose. My client—a fast-moving clinical-stage biotech—is searching for a TMF Specialist who can bring structure, clarity, and inspection-ready excellence to their growing pipeline. If you love organizing the...SuggestedHourly payContract workImmediate start
$25 - $32 per hour
We are seeking a highly organized TMF Coordinator to support the management of the Trial Master File (TMF) within Veeva Vault eTMF. This role ensures TMF completeness, accuracy, and inspection readiness, working closely with study teams, TMF leads, and external partners...SuggestedHourly payLong term contractFull timeWork at office- Role Summary The TMF Document Specialist is responsible for owning and overseeing the management and quality control of Trial Master File (TMF) documentation across multiple Phase I-IV global studies. This hands‑on role involves leadership in document management processes...Suggested
- ...currently hiring individuals seeking an exciting career in clinical research, managing our Trial Master File. The Trial Master File (TMF) is a collection of documents that stores all data and research collected on a given trial. The TMF allows us to conduct a clinical trial...SuggestedContract workCurrently hiringLocal areaImmediate startFlexible hours
- ...TMF Documentation Coordinator A Few Words About Us - Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its...Suggested
$52k - $54.9k
The McKnight Foundation is seeking a professional Program Team Administrator (PTA) to support the goals of its Arts, Vibrant & Equitable Communities, and other grantmaking programs. Reporting to the Grants & Information Manager, this role is crucial as the Foundation advances...SuggestedFull timeContract workWork experience placementWork at office$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 clinical research organization is seeking candidates for an office-based position managing the Trial Master File in Cincinnati, OH. The role involves overseeing trial documentation and ensuring data integrity. Qualified candidates should have an Associate ’s degree, strong...Suggested
- ...years in a clinical study environment, possess strong organizational and communication skills, and hold a degree in an administrative or scientific field. This position offers competitive salary and benefits in a collaborative work environment. #J-18808-Ljbffr Ipsen GroupSuggested
- A clinical research organization is seeking a Clinical Records Administrator to support TMF oversight in Cincinnati, Ohio. Responsibilities include managing electronic filing systems, tracking documents, and ensuring quality standards are met. Ideal candidates have an associate...SuggestedFlexible hours
- ...serve as a technical and operational partner to the sales team. You will drive business growth through expert demonstrations of the TMF suite and provide client advocacy within the organization. This role requires exceptional communication skills and a high degree of initiative...Suggested
- ...professional to join a well-known client’s team in California as a TMF/Sr. TMF Specialist. This remote role will provide primary support... ...of the TMF content Follow up with the appropriate functional group or document owner to mitigate, as per the established review schedule...SuggestedRemote jobLocal areaImmediate start
- ...themselves and are inspired to do their best work every day. Join us! What Records Management Compliance Department Does At Worldwide TMF Operations handles the processing, maintenance and archiving of all essential documents in strict accordance with pertinent Standard...SuggestedRemote jobWorldwide
- A leading biotech company in Boston is seeking a TMF Document Specialist to oversee the management and quality control of Trial Master File documentation. This role involves ensuring compliance with regulatory requirements and leading document management processes for multiple...
- A biotech company is seeking a TMF Document Specialist to manage trial master file documentation for clinical studies. This role includes overseeing document management processes, ensuring compliance with regulatory standards, and collaborating with cross-functional teams...
- A healthcare solutions company in Basking Ridge, NJ is looking for a Clinical Study Associate I to assist in clinical study planning and execution. Candidates should have at least 1 year of relevant experience, including familiarity with Veeva. The position involves providing...Contract work
- A leading clinical research organization is seeking a TMF Operations role in Georgia. This role requires strong data collection and communication skills, along with proficiency in Microsoft Office. The successful candidate will process and manage critical trial documents...Work at officeWorldwide
- A biopharmaceutical company is seeking a TMF Associate to manage day-to-day Trial Master File operations within Veeva Vault. Responsibilities include maintaining accurate study data, managing site records, and ensuring TMF quality and readiness for inspections. The ideal...
- A clinical research organization in Georgia is seeking a TMF Operations professional to fulfill the TMF Approver role and ensure compliance with document processing standards. The ideal candidate should possess a university degree, relevant skills in data handling, and...Worldwide
$41.6k - $56.16k
Piper Health & Sciences is seeking a TMF Specialist t o join a leading full-service Contract Research Organization (CRO) located in the greater Washington, DC/Montgomery County area. The TMF Specialist will support Trial Master File (TMF) activities across clinical trials...Hourly payFull timeContract workRemote work3 days per week- A clinical research organization in Cincinnati is hiring for a role managing the Trial Master File. Responsibilities include overseeing documentation quality, tracking electronic documents, and communicating with global teams. Candidates should have an associates degree...Work at office
- A biopharmaceutical oncology company is seeking a TMF Associate to manage the Trial Master File within Veeva Vault. The role includes maintaining accurate study data, ensuring TMF completeness, and supporting cross-functional teams. Candidates should possess 1-3 years of...
- A leading clinical development organization is seeking a TMF/Sr. TMF Specialist for a remote position in California. The role involves ensuring adherence to regulatory requirements and maintaining the Trial Master Files (TMF) inspection readiness. The ideal candidate will...Remote job
- A leading Contract Research Organization in the greater Washington, DC area is seeking a TMF Specialist to oversee Trial Master File activities across clinical trials. This full-time, hybrid role involves ensuring regulatory compliance, conducting quality control, and using...Full timeContract work
- A leading pharmaceutical company in Basking Ridge, New Jersey is seeking a dedicated individual to assist in planning and executing clinical trials. The role involves supporting interactions with Contract Research Organizations (CROs) and managing trial documents in compliance...Contract work
$100k - $125k
...least 5 years of clinical research experience and 2 years of onsite monitoring/site management experience. Responsibilities include TMF management, document quality control, and support for study leads in meeting compliance with clinical protocols. Competitive salary range...- A leading healthcare solutions provider is looking for a TMF Inside Sales Representative to identify and qualify opportunities for their TMF-Technology and Services Solutions. This full-time role is ideal for individuals with 2-3 years of sales experience, strong communication...Full time
- 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...