Senior RIM Lead: Veeva

A leading technology consultant is seeking an experienced Veeva Regulatory Information Management (RIM) professional to lead global regulatory operations and system implementations. The ideal candidate will have 8–12 years of experience, strong hands-on experience with Veeva RIM and Ennov, and the ability to work across regulatory teams. Responsibilities...

Lead - Regulatory Information Management 1 day ago Be among the first 25 applicantsThis role is for one of the Weekday's clients. Minimum experience: 8 years. Location: Europe. Job type: full-time.We are seeking an experienced Veeva Regulatory Information Management (RIM) professional with strong expertise in Ennov to lead and support global regulatory...

Lead - Regulatory Information Management1 day ago Be among the first 25 applicantsThis role is for one of the Weekday's clients. Minimum experience: 8 years. Location: Europe. Job type: full-time.We are seeking an experienced Veeva Regulatory Information Management (RIM) professional with strong expertise in Ennov to lead and support global regulatory...

This role is for one of the Weekday's clientsMin Experience: 8 yearsLocation: EuropeJobType : full-timeWe are seeking an experienced Veeva Regulatory Information Management (RIM) professional with strong expertise in Ennov to lead and support global regulatory operations and system implementations. The ideal candidate will play a critical role in managing...

This role is for one of the Weekday's clients Min Experience: 8 years Location: Europe JobType : full-time We are seeking an experienced Veeva Regulatory Information Management (RIM) professional with strong expertise in Ennov to lead and support global regulatory operations and system implementations. The ideal candidate will play a critical role in...

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 Documentation & Records Management LeadJoin to apply for the Clinical Trial Documentation & Records Management Lead role at Chiesi GroupBased 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...

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...

Senior Enterprise Sales Software solutions Lead ItalyJob Description As a Sr

A leading technology company in Italy is seeking a Senior Enterprise Sales Software solutions Lead. In this role, you will manage strategic accounts, develop