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 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...

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...

Business Consultant - Commercial Strategy (Remote) Pay Competitive Employment type: Other Job Description Veeva Systems is a mission-driven organization and pioneer in industry cloud, helping life sciences companies bring therapies to patients faster. As one of the fastest-growing SaaS companies in history, we surpassed $2B in revenue in our last fiscal year...

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...

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...

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...

Join a pioneering organization in the life sciences sector as a Business Consultant, where you'll lead consulting projects that drive digital and commercial innovation. This role offers the flexibility to work remotely, allowing you to thrive in your ideal environment. You'll engage with top pharmaceutical companies, solve complex problems, and develop...

CPL & TAYLOR by Synergos is recruiting: SENIOR DIGITAL REGULATORY CONSULTANT LIFE SCIENCES (Ref. ANN ) Location: full remote Contract: Permanent, full-time Compensation: To be defined based on experience The Company A leading international organization specializing in consulting and digital solutions for the Life Sciences sector, with headquarters in Italy....