Regulatory Affairs Associate Director Job. My Client a Global CRO is seeking an Associate Director for its Cambridge office.
Providing discovery, development and post-approval services to pharmaceutical, biotechnology, medical device, academic and government organisations.
The Associate Director of Regulatory Affairs will be responsible for providing direct management and support to members of the Regulatory Affairs Strategic team in Cambridge.
A key aspect of this role is that you will act as the Executive contact for the sponsor to oversee and ensure all aspects of Regulatory Affairs are conducted in accordance with their requirements
The Role
This role is based at their European head office in Cambridge with the successful applicant responsible for providing direct management and support to members of the Regulatory Affairs Strategic team.
They will also be responsible for all budgets and contracts in relation to their assigned projects. This position directly relates to the development and securing of new business opportunities, and the day to day operational management of assigned regulatory services in accordance with contract, all applicable regulatory requirements and laws, and appropriate policies and procedures.
The Person
Candidates will be able to demonstrate good in-depth knowledge in either the preclinical, CMC or clinical environment and should possess the ability to motivate and integrate teams and teach/mentor team members. They should have broad Regulatory Affairs experience, excellent knowledge of ICH and European/ROW Regulatory Procedures, including both clinical trials and product licensing and proven success in agency influencing and negotiation
I am a specialist recruiter for the regulatory affairs field within the pharmaceutical industry. I have positions with the top biotech, pharma, CRO and consultancies in the UK. If this is a position which is of interest to you please contact David Nixon at Hays Pharma on +44 (0)207 633 4813
This job was posted 30+ days ago, and has expired.
