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, cross-functional collaboration, and strategic vendor management. Join us to enhance the oversight and integrity of clinical studies while making a significant impact in the field. #J-18808-Ljbffr



  • WorkFromHome, Italia Chiesi Farmaceutici S.p.A. A tempo pieno

    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...


  • 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...


  • WorkFromHome, Italia Chiesi Group A tempo pieno

    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...


  • 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...


  • WorkFromHome, Italia Chiesi Farmaceutici S.p.A. A tempo pieno

    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 eTMF and CTMS. This role emphasizes team leadership,...

  • Clinical Trial Docs

    6 giorni fa


    Workfromhome, Italia Chiesi Group A tempo pieno 90.000 €

    A global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead. This role requires leadership in managing clinical documentation and records, ensuring compliance with regulatory standards, and overseeing clinical trial technologies. Candidates should have 8-10 years of experience in clinical...

  • Clinical Trial Docs

    3 settimane fa


    WorkFromHome, Italia Chiesi Group A tempo pieno

    A global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead. This role requires leadership in managing clinical documentation and records, ensuring compliance with regulatory standards, and overseeing clinical trial technologies. Candidates should have 8-10 years of experience in clinical...


  • WorkFromHome, Italia Chiesi Group A tempo pieno

    A global pharmaceutical company based in Parma, Italy is seeking a Clinical Trial Documentation & Records Management Lead. This role requires leadership in managing clinical documentation and records, ensuring compliance with regulatory standards, and overseeing clinical trial technologies. Candidates should have 8-10 years of experience in clinical...


  • WorkFromHome, Italia ICON A tempo pieno

    A leading healthcare intelligence organization is seeking a Clinical Site Associate to support clinical trial operations. The role requires managing site communications, coordinating trainings, and maintaining essential documentation. Ideal candidates will have a Bachelor's in life sciences, experience in clinical research, and strong organizational skills....

  • Sr Clinical Trial Manager

    2 settimane fa


    WorkFromHome, Italia Syneos Health, Inc. A tempo pieno

    Sr. Clinical Trial Manager (Clinical Research Medical Advisor) - FSP - Homebased Updated: October 15, 2025Location: BRA-RemoteJob ID: Description Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to...