Expiry Date: 17-02-2020
Category Regulatory Affairs
Salary: On Application
Job Type: Full Time
Director, CMC Regulatory Affairs - across all development phases (I-III) – London
Location: Central London, England
As Regulatory Affairs CMC Director or Associate Director you will provide CMC support for regulatory aspects of submissions for products across all development phases (I-III).
This is a great opportunity to join the London based European Head office of my established but still rapidly expanding global Pharmaceutical client, which has a strong culture of innovation and staff development. The company has grown to become a major research-driven pharmaceutical company across a number key and highly interesting therapeutic areas and is now expanding its EMEA Regulatory Affairs CMC team.
Benefits: The role comes with flexible working hours, options for working from home, company car parking available, great holiday allowances, a high basic salary, bonus up to 20% per year, company car allowance, valuable stock options, full medical and healthcare coverage and insurances for you and your family.
Role / Description: As Regulatory Affairs CMC Director or Associate Director you will provide CMC support for regulatory aspects of submissions for products across all development phases (I-III) and MAA registration applications, PIPs, scientific advice and pre-submission meetings, response to questions and the planning and preparation of Quality sections of IMPDs.
This is a great role where you will have full autonomy, scope and leadership for your projects. This is NOT a US centric organisation, this is a role and organisation where the EU leads its own development and submission plans.
To apply for this role, please press the red “Apply for position” button, or contact Theo Moore on +44 (0)207 801 3384 or Oli Dimitrov on +44 (0)207 801 3388 in full confidence to receive more details on this role or to hear about other available opportunities in Regulatory Affairs.
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