Expiry Date: 17-08-2020
Category Regulatory Affairs
Salary: On Application
Job Type: Full Time
Global Regulatory Director, reports to PL (mAb, EOP2 / global RA strategy role)
This role is in Mainland Europe and comes with a full relocation, including private schooling (where the company has a policy on eligibility) and a tax ruling.
About the Opportunity
This is a role with a mid-sized biopharma company with 4 or so therapy areas and with a long track record of bringing new medicines to market. This is not a top 5 or top 10 pharma company, but leaner, smaller, and more agile.
The role is a Global Strategy Lead so you will take an EOP2 asset through Ph 3 and into BLA, and lead the regulatory sub team through to parallel submissions in all the core markets, and for the first wave of the international majors. Uniquely, this role reports to the PL, so you will be based in the same site as the PL and work directly in his team.
The client would like an individual who has been a GRL before, so this means, you might have led a s/NDA or NDA (but where the local sub was done by your US liaison), or you have been highly exposure to US framework, and know the US pathway well.
You will be a focused individual, who lives and breathes drug development, the vision you have for your molecule and know how to balance risk with innovation.
About the Molecule
The NME is a mAb, in a disease area which is highly debilitating and as yet, not properly met with treatment options.
Package & Relocation
You want to benefit from a stock and bonus package, which keeps you engaged and also a career path which keeps you on your toes in a positive way! My client offers RSU based stock, car allowance and performance bonus, and will entertain buying out existing bonus / stock plans (within reason). They offer a full relocation subject to their policy if you want to move to be near the site.
To apply for this role, please press the red “Apply for position” button, or contact Oli Dimitrov on +44 (0)207 801 3388 or Theo Moore on +44 (0)207 801 3384 in full confidence to receive more details on this role or to hear about other available opportunities in Regulatory Affairs.
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