Overview
Reference Number: JO-2307-519468
Vice President Regulatory Affairs
Rate: Negotiable
Job Type: Permanent
Location: Oxford
Vice President of Regulatory Affairs
Offering a lucrative Salary and Benefit package
Oxford based – flexible working available
A fantastic opportunity has become available with an innovative biotech who support in the discovery and development of immunotherapeutic products and vaccines. Currently looking for a Vice President of Regulatory Affairs this is opportunity is perfect for a strong strategic regulatory leader who has extensive experience working as a strategic decision maker.
Job Responsibilities include;
Strategic leadership of the global regulatory affairs team.
Build and nurture relationships with Health Authorities for successful interactions and outcomes, acting as the company’s primary point of contact.
Act as an independent subject matter expert to various project teams and departments, with particular close collaboration with the clinical operations and research departments.
Keep abreast of global regulatory requirements and assessing risks, developing contingency plans.
Overseeing coordination of regulatory submissions, strategizing for dossier updates, and submission of new INDs/CTAs/NDAs/MAAs.
Candidate Requirements include;
Eligibility to live and work in the United Kingdom
A Life Sciences degree or equivalent university degree
A minimum of 10-15 years global Regulatory experience supporting UK & China affiliates
Previous vaccines experience is highy desirable
Proven expertise in regulatory submission and approval processes, and in resolving complex CMC regulatory issues
If this opportunity is of interest to yourself please forward your up to date CV to Sophie on sophie.malyon@cpl.com.
