Senior RIM Lead: Veeva

Lead - Regulatory Information Management 1 day ago Be among the first 25 applicants This 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...

A community living organization in Italy is seeking a Lead Resident Services Associate who will serve as a point of contact for residents, manage requests, and coordinate services. The ideal candidate should have a strong background in customer service, preferably with experience working with seniors. Full benefits include medical, dental, vision, life...

A community living organization in Italy is seeking a Lead Resident Services Associate who will serve as a point of contact for residents, manage requests, and coordinate services. The ideal candidate should have a strong background in customer service, preferably with experience working with seniors. Full benefits include medical, dental, vision, life...

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...

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 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...

A leading healthcare company is looking for a Data Team Lead / Senior Data Team Lead to manage end-to-end delivery of data management services. Responsibilities include ensuring quality deliverables, managing client relationships, and providing comprehensive expertise to the Clinical Data Management team. The ideal candidate will have over 5 years of...

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...