Trial Master File Associate
1 giorno fa
3 giorni fa Join Our Team as a Trial Master File Associate - home based in Poland, Italy or Israel or hybrid in Barcelona, Spain About this role As part of our CDS Ophthalmology Trial Master File team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. The Trial Master File Associateis is part of the TMF Delivery Business Line within Clinical Development Services (CDS) and will function operationally as a member of the Study Team with the responsibility to organize, maintain and oversee the Trial Master File (TMF) according to company policies, SOPs, Work Instructions, regulatory requirements, TMF Functional Lead and PM delegation. Key Responsibilities : Notify study team that TMF is created and ready for document upload for eTMF or submission to pTMF Develop TMF Plan Provide training on study specific TMF requirements, guidelines including TMF Plan Perform QC2 on documents and documents reconciliation Provide TMF Monthly Reports to PM, Line manager and Head of TMF Delivery Regularly check TMF metrics, follow up on detected issues, ensure acceptable level of metrics Ensure TMF processes timely implementation and execution Adjusting study specific TMF Index / EDL in the relevant files / system as directed by the PM (Project Manager) Ensure valid forms and templates are implemented and maintained in the assigned projects Check status of duplicates, documents in error, size and path length (if applicable), follow up on necessary corrections accordingly Coordinate Monthly and Quarterly TMF Reconciliation by creating Action Plan and submitting relevant report on the status Ensure TMF AoR completion and monitoring TMF
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Trial Master File Associate
2 settimane fa
WorkFromHome, Italia European Institute of Policy Research and Human Rights SIA A tempo pienoRemoto EUR 50.000 - 70.000 2 giorni fa TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service‑capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a...
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Trial Master File Associate
1 giorno fa
WorkFromHome, Italia Gain.pro A tempo pienoJoin Our Team as a Trial Master File Associate - home based in Poland, Italy or Israel or hybrid in Barcelona, Spain About this role As part of our CDS Ophthalmology Trial Master File team you will working alongside passionate and innovative professionals to ensure our customers achieve their goals. The Trial Master File Associateis is part of the TMF...
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Trial Master File Associate
58 minuti fa
WorkFromHome, Italia TFS HealthScience A tempo pienoTFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Trial Master File Associate - home based...
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Trial Master File Associate
2 settimane fa
WorkFromHome, Italia European Institute of Policy Research and Human Rights SIA A tempo pienoRemoto EUR 50.000 - 70.000 2 giorni fa TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service‑capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a...
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TMF Specialist — Trial Master File
2 settimane fa
WorkFromHome, Italia European Institute of Policy Research and Human Rights SIA A tempo pienoA global Contract Research Organization is seeking a Trial Master File Associate to work remotely or hybrid. The role involves managing the Trial Master File and ensuring compliance with TMF processes. The candidate should have 1-5 years of relevant experience, preferably in CRO or Pharmaceutical sectors, and must demonstrate strong organizational skills and...
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Trial Master File Associate
1 settimana fa
WorkFromHome, Italia Ashby A tempo pieno3 giorni fa TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service‑capabilities, resourcing and Functional Service (FSP) solutions. Join Our Team as a Trial Master File...
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TMF Master File Associate — Remote/Hybrid Europe
1 settimana fa
WorkFromHome, Italia Ashby A tempo pienoA leading Contract Research Organization is seeking a Trial Master File Associate to manage the Trial Master File (TMF). The role involves organizing and maintaining TMF compliance according to regulations and collaborating with study teams. Ideal candidates have TMF management experience and a Bachelor's degree in Health Science. This position offers...
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WorkFromHome, Italia Gain.pro A tempo pienoA global healthcare-focused organization is seeking a Trial Master File Associate to manage the Trial Master File in a flexible hybrid work model. The role requires at least 3 years of experience in TMF management, preferably within ophthalmology, and a degree in a related field. Responsibilities include organizing TMF documentation, training study teams,...
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TMF Master File Associate
1 giorno fa
WorkFromHome, Italia TFS HealthScience A tempo pienoA leading global Contract Research Organization is seeking a Trial Master File Associate to manage and oversee TMF processes. This role involves developing TMF plans, ensuring the submission readiness of documentation, and training the study team on TMF requirements. Qualified candidates will have at least 3 years of TMF experience, preferably in the...
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Remote TMF Associate
1 giorno fa
WorkFromHome, Italia Iriscube Reply A tempo pienoA global Contract Research Organization is seeking a Trial Master File Associate. This role involves managing the Trial Master File, ensuring compliance, and collaborating with study teams to facilitate documentation processes. Applicants should have 1-5 years of experience in the CRO or pharmaceutical industry, with a mandatory 3 years of TMF experience....
