Expiry Date: 10-10-2019
Category Regulatory Affairs
Salary: On Application
Job Type: Full Time
Regulatory / Regulatory Affairs CMC Associate Director / London
Regulatory Affairs CMC Associate Director role for a London based global Pharmaceutical company who are rapidly expanding, with a strong development pipeline.
Location: London, Greater London
Based in Central London, you have the option of driving (parking available) or commuting via train, as there are number of tube stations within 10mins, so all the advantages of working in central London will be available to you! There is also great flexibility on start and finish times and good options to work 2 days a week from home.
The pipeline is strong at my Pharmaceutical client and operating as the Regulatory Affairs CMC Associate Director, you will take the leadership for products/indications in Phases I & II as the regulatory CMC leader, authoring and preparing IMPD’s after receiving the data from different regions, with the option to take your products through late stage development as well.
The structure and cultural here are relaxed, and Regulatory Affairs CMC leaders have full autonomy for their products (stratergy development, HA meetings, leasing with the Clinical Group, cross functional meetings etc.), so soft skills are most important. The London EU HQ is small but still growing (with most of the other technical teams also based at the London site), and as the company grows there will be more opportunities for career growth and working from home - this is actually a great place to work for people with families.
On offer is a great salary, with bonus, car allowance, share options, and fully comprehensive healthcare package for you and your family including medical and life insurance. Flexible working hours are available to all, and there are also good options to work 2 days a week from home.
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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