Job Title: Principal Consultant (Embedded as Regulatory Affairs Director)
Location: Homebased UK or Europe
Attractive package including bonus, car allowance, range of benefits
This is a fantastic opportunity to work with one of the worlds leading consultancy divisions, embedded into a Top 3 Pharmaceutical business as a Regulatory Affairs Director, leading developing oncology programs globally.
As a Principal Consultant you will be client dedicated and embedded into a global pharma, driving the development and commercialisation of an innovative oncology portfolio, taking lead on regulatory strategy, health authority interactions and drug development activities.
Responsibilities:
-Development and implementation of global regulatory strategy
-Lead regulatory interactions and the review processes in local region
-Ability to advocate persuasively to senior leaders internally and to health authorities
-Lead drug development activities for Oncology portfolio
Experience:
-Strong drug/clinical development background
-Ideally Oncology experience or innovative therapeutic area
-Experience leading regional development, submission, and approval activities
If youre interested in discussing this role further, please apply with an updated version of your CV and I will be in touch to discuss further chris.bart@cpl.com
- Agency: Cpl Life Sciences
- Reference: JO-2205-492493
Website: Cpl Life Sciences
- Posted: 7th June 2022
- Expires: 5th July 2022
