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.
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