Clinical Trial Documentation
2 giorni fa
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, 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
-
Clinical Trial Documentation
5 ore fa
Parma, Emilia-Romagna, Italia Chiesi Farmaceutici S.p.A. A tempo pienoDate: 19 Dec 2025Department: 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 healthcare group with 90 years' experience, operating in 31 countries with more than...
-
Clinical Trial Documentation
5 ore fa
Parma, Emilia-Romagna, Italia Chiesi Group A tempo pienoAbout usBased 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 achieve its mission of improving people's quality of life by acting responsibly towards society and the environment, the Group researches,...
-
Clinical Trial Documentation
3 settimane fa
Parma, Italia Chiesi Farmaceutici S.p.A. A tempo pienoSelect 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...
-
Clinical Trial Documentation
3 settimane fa
Parma, Italia Chiesi Farmaceutici S.p.A. A tempo pienoSelect 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...
-
Clinical Trial Documentation
2 giorni fa
Parma, Italia Chiesi Farmaceutici S.p.A. A tempo pienoSelect 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...
-
Clinical Trial Documentation
3 settimane fa
parma, Italia Chiesi Farmaceutici S.p.A. A tempo pienoSelect 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...
-
Clinical Trial Documentation
2 settimane fa
Parma, Italia Chiesi Farmaceutici S.p.A. A tempo pienoA 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 Documentation
3 settimane fa
Parma, Italia Chiesi Farmaceutici S.p.A. A tempo pienoA 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 Administrator
2 settimane fa
Parma, Italia IQVIA A tempo pienoOn 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 pienoWho we are looking for Purpose The Senior Clinical Research Physician provides scientific and strategic leadership in the design, execution, and interpretation of global clinical studies in the non-obstructive respiratory diseases therapeutic area. They will drive the preparation of documents for regulatory submissions, ensuring the scientific validity and...