Senior Consultant - Regulatory Affairs
NNIT is one of the world’s leading consultancies for the past twenty years serving the Life Science industry around the world. We strive to enable our customers to achieve their business goals through digitalization within Quality Assurance, Regulatory Affairs, Clinical, Pharma Production and Laboratory processes.
To further strengthen our Regulatory Affairs team, we are looking for a Senior Consultant with a diverse skill set across Regulatory Affairs in the life sciences industry including some IDMP regulatory affairs exposure.
Your 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, contribute to business development and sales activities and contribute to and deliver Requests for Proposal (RFP’s) as required.
On average you will split your time:
75% delivering in consultancy projects in advisor,
project lead or architect roles, and acting as engagement delivery lead.
10% in business development, presales and though leadership activities
10% in the development and delivery of RFP’s to ensure NNIT successfully engages new and additional projects
5% in coaching and mentoring of more junior consultants in the Regulatory Affairs team
Your qualifications and experience:
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
📌 Senior Consultant (España)
🏢 NNIT
📍 España