Trial Master File Jobs
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Search Results - Trial Master File Jobs
Cincinnati-medpace.com-
Job Summary:
We are currently hiring entry-level 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...
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Syneos Health, Inc.-San Juan-appcast.io-
timeliness and completeness. Reconciles contents of the ISF with the Trial Master File (TMF). Ensures the investigator/physician site is aware of the requirement of archiving essential documents in accordance with local guidelines and regulations...
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Cincinnati-medpace.com-
Job Summary:
We are 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...
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Adecco-Richmond-adecco.com-
Identify study risks, trends, and site performance issues and implement corrective actions or escalation plans as appropriate.
• Support Trial Master File (TMF) management by ensuring accurate, complete, and inspection-ready documentation.
• Coordinate...
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Abbott Laboratories-Alameda (CA)-jobs.abbott-
and training of investigator sites, planning and running study meetings, evaluation, selection and training of new study investigators and writing and assembling submissions.
• Maintain and audit Trial Master File to ensure inspection readiness.
• Perform...
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Flourish Research-Century (CA)-workable.com-
guidelines and FDA regulatory requirements
• Familiarity with Trial Master File structure, document filing standards, and audit-readiness best practices
• Experience with electronic document management and signature platforms, such as Veeva Vault, Trial...
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Randstad-San Rafael (CA)-randstadusa.com-
Capture (EDC), Trial Master File (TMF), Electronic Trial Master File (eTMF)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status...
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Cincinnati-medpace.com-
Job Summary:
We are currently hiring entry-level 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...
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Boulder-icims.com-
and all documentation required for the Trial Master File
• Responsible for maintaining and completing Case Report Forms in agreement with the source documentation and in accordance with the study protocols
• Assures clinical supply accountability...
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Meditrial Europe Ltd.-Minneapolis-allibo.com-
but not limited to, conduct of the trial kick-off meeting, the set-up of trial master file (TMF), site selection and finalization of site and vendor Clinical Trial Agreements (CTAs) and budgets.
Ensure effective project plans are in place and operational for each...
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IUVO BIOSCIENCE OPERATIONS, LLC-Rochester-gnahiring.com-
impacts.
• Drive issue resolution and continuous process improvement.
• Responsible for meeting and communicating project timelines and budget internally and with client.
• Oversee delivery of a clean and complete Trial Master File (TMF).
• Work directly...
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Princeton (NJ)-pharmiweb.jobs-
Supports maintenance of inspection-ready Trial Master File (TMF) according to ICH-GCP and company SOPs
• Performs quality checks on the study TMF with oversight of study Clinical Operations Lead (COL)
• Assists in the preparation of study related...
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Pfizer-New York-dejobs.org-
EDC) system and/or other data collection systems.
+ Ensure work carried out in accordance with applicable SOPs and working practices.
+ Ensure the required study-specific CDS documents in the Trial Master File (TMF) are of high quality...
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VIDA Diagnostics-Coralville-prismhr-hire.com-
and associated acquisition parameters.
• Knowledge of 21 CFR 812 (medical device regulations) and/or ISO 13485
• Experience with clinical trial management systems (CTMS), electronic trial master files (eTMF), or imaging data platforms (e.g., Medidata, Veeva...
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Cincinnati-medpace.com-
to regulatory issues.
Responsibilities :
• Provide support to the study start-up team through completion of compliance tasks
• Maintain and perform ongoing quality review of trial documents within the Trial Master File (TMF);
• Gain hands-on training...
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