TMF Specialist — Trial Master File
7 giorni fa
A 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 teamwork ability. This position offers a competitive compensation package and opportunities for personal and professional growth in a collaborative environment.#J-18808-Ljbffr
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Trial Master File Associate
7 giorni 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 settimana 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...
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TMF Master File Associate — Remote/Hybrid Europe
2 giorni 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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TMF Master File Associate
1 settimana 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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Trial Master File Associate
7 giorni 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
2 giorni 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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Trial Master File Associate
1 settimana 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...
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Clinical Trial Documentation
6 giorni fa
Workfromhome, Italia Chiesi Group A tempo pieno 90.000 €Clinical Trial Documentation & Records Management Lead Join to apply for the Clinical Trial Documentation & Records Management Lead role at Chiesi Group Based in Parma, Italy, Chiesi is an international research-focused pharmaceutical and healthcare group with 90 years’ experience, operating in 31 countries with more than 7,000 employees (Chiesi Group). To...
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Clinical Trial Documentation
6 giorni fa
Workfromhome, Italia Chiesi Farmaceutici S.p.A. A tempo pieno 90.000 €Select how often (in days) to receive an alert: Clinical Trial Documentation & Records Management Lead Department: Global Clinical Development Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT About us Based in Parma, Italy, Chiesi is an international research-focused...
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Clinical Trial Documentation
6 giorni fa
Workfromhome, Italia Chiesi Farmaceutici S.p.A. A tempo pieno 90.000 €A leading pharmaceutical company in Parma, Italy, seeks a Clinical Trial Documentation & Records Management Lead to ensure compliance with regulatory standards and manage clinical trial technologies. The ideal candidate has 8-10 years of experience in clinical operations and a robust understanding of e TMF and CTMS. This role emphasizes team leadership,...