02 ago - Italia
NNIT
Senior Consultant - Regulatory Affairs Location: UK, Denmark, Spain, Italy, Germany, Poland, Czech, Ireland, Switzerland Type of contract: Permanent Language(s): English Mobility: Some Travel (Application Deadline: 31/07/2026 Responsibilities You will join our Regulatory Affairs team as a Senior Consultant. You will contribute to forming a variety of tasks and functional responsibilities within the Regulatory Affairs business unit such as taking ownership of client engagements and specific projects, contributing to business development and sales activities and contributing to and delivering Requests for Proposal (RFP's) as required. On average you will split your time as follows: 75% delivering in consultancy projects in advisor, project lead or architect roles and acting as engagement delivery lead. 10% in business development, presales and thought leadership activities. 10% in the development and delivery of RFP's to ensure NNIT successfully engages new and additional projects. 5% coaching and mentoring of more junior consultants in the Regulatory Affairs team.
Essential Requirements A Bachelor's Degree (or similar) in a field related to Pharmaceutical Compliance or Regulation. Other relevant academic qualifications can be considered if you also have highly significant consulting and/or industry based experience in Regulatory Affairs within Life Sciences. Significant experience in Regulatory Affairs within a Pharmaceutical company or as a consultant. Proven consulting based experience is an essential requirement for the role, ideally within a large recognised consultancy with a life sciences division or specialism. A proven level of experience in the area of IDMP, including: Experience in IDMP data transformation; data enrichment for PMS, RIMS and XEVMPD; experience with RIM systems related to IDMP; fully aware and cognizant of current EMA updates on IDMP; experience presenting IDMP topics to larger audiences; proficiency in PMS and Postman API. Experience managin
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dalia2