Are you an expert in IDMP or RIMs Regulatory Affairs, looking to make a substantial impact on innovative projects in the life sciences sector? Our client, with a rapidly expanding portfolio, seeks Consultants to advance excellence in IDMP processes and RIMs technology.

Key Responsibilities:

• Partner with clients on IDMP process improvements, RIMs initiatives, data governance, and data quality projects.
• Advise clients on regulatory requirements and technologies, including systems like Veeva Vault RIM.
• Participate in business development to support our Regulatory Affairs expansion.
• Collaborate with various stakeholders to strengthen the company's strategic goals in RA.

Essential Qualifications:

• MSc in life sciences or IT with significant experience in RA or consultancy, focusing on IDMP or RIMs.
• Preferably a background in management consulting or advisory roles.
• Strong IT understanding and its application in RA for successful implementations.
• Experience with agile delivery methods, such as SAFe, is beneficial.
• Knowledge of regulatory business processes and the advantages of digitisation.
• Proficiency in English is essential.

Location:

• This role can be performed remotely from the UK and most EU countries.

Interested? Send your resume to or contact 020 7940 1212 to explore these exciting opportunities.