Lavori attuali relativi a Hybrid Lead: Clinical Trial Documentation - Parma - Chiesi Farmaceutici S.P.A.


  • Parma, Italia Chiesi Farmaceutici S.P.A. A tempo pieno

    A leading pharmaceutical company is seeking a Clinical Trial Documentation & Records Management Lead in Parma, Italy. This role involves establishing and improving the documentation unit, ensuring compliance with regulatory standards. Ideal candidates will have 8-10 years of clinical operations experience, strong leadership skills, and knowledge of eTMF and...


  • Parma, 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...


  • Parma, 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...


  • parma, Italia Chiesi Farmaceutici S.P.A. A tempo pieno

    Select how often (in days) to receive an alert :Clinical Trial Documentation & Records Management LeadDepartment : Global Clinical DevelopmentBusiness Area : R&D, Pharmacovigilance & Regulatory AffairsJob Type : Direct EmployeeContract Type : PermanentLocation : Parma, ITAbout usBased in Parma, Italy, Chiesi is an international research-focused...


  • Parma, 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...


  • parma, Italia Chiesi Farmaceutici S.P.A. A tempo pieno

    Select how often (in days) to receive an alert :Clinical Trial Documentation & Records Management LeadDepartment : Global Clinical DevelopmentBusiness Area : R&D, Pharmacovigilance & Regulatory AffairsJob Type : Direct EmployeeContract Type : PermanentLocation : Parma, ITAbout usBased in Parma, Italy, Chiesi is an international research-focused...


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

    Select how often (in days) to receive an alert:Clinical Trial Documentation & Records Management LeadDepartment: Global Clinical DevelopmentBusiness Area: R&D, Pharmacovigilance & Regulatory AffairsJob Type: Direct EmployeeContract Type: PermanentLocation: Parma, ITAbout usBased in Parma, Italy, Chiesi is an international research-focused pharmaceutical and...


  • Parma, 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,...


  • Parma, Italia IQVIA A tempo pieno

    On behalf of our Client a global pharmaceutical company, IQVIA is looking for **a e-TMF Specialist - Supply section** who can join an exciting working environment in a dynamic atmosphere. **RESPONSIBILITIES**: - To review eTMF plans - To upload documents in the eTMF and perform ongoing quality control of the eTMF (Investigational products and Clinical...


  • Parma, Italia Chiesi Group A tempo pieno

    A global pharmaceutical company in Parma, Italy, seeks a Clinical Pharmacologist Lead with over 5 years of industry experience to oversee clinical pharmacology strategies. Responsibilities include leading Clinical Development Programs, designing trial protocols, and integrating innovative methodologies. The ideal candidate will have an MD or PhD, proven...

Hybrid Lead: Clinical Trial Documentation

1 ora fa


Parma, Italia Chiesi Farmaceutici S.P.A. A tempo pieno

A leading pharmaceutical company is seeking a Clinical Trial Documentation & Records Management Lead in Parma, Italy. This role involves establishing and improving the documentation unit, ensuring compliance with regulatory standards. Ideal candidates will have 8-10 years of clinical operations experience, strong leadership skills, and knowledge of eTMF and CTMS systems. Flexible hybrid working arrangements are available. The company promotes continuous training and a supportive working environment with a focus on work-life balance.#J-18808-Ljbffr