Regulatory Affairs Director

Job Title: Regulatory Affairs Director
Contract Type: Permanent
Location: Dublin
REF: 123340
Contact Name: Director of The RFT Group
Contact Email:
Job Published: almost 4 years ago

Job Description

Regulatory Affairs Director

Our client is a fast growing highly profitable multinational biopharmaceutical company with an exciting pipeline of drug compounds at an advanced stage in research. With a hugely experienced and successful executive management team this company has a newly created vacancy for an experienced Regulatory Affairs Director.This newly created senior management position will be located in Dublin with flexibility to work from home.

Job Purpose
The Regulatory Affairs Director will be responsible for the development and implementation of regulatory strategy of the company’s European development projects. The Regulatory Affairs Director will sit of a number of global development teams with involvement in US related projects.
Duties and Responsibilities
  • Responsible for working with the project team to identify an optimum European regulatory strategy for assigned projects. Able to lead teams in examining regulatory strategy options.
  • Expected to independently interact with regulatory authorities, and outside consultants when needed. Able to independently prepare and lead a team through a European Health Authority regulatory meeting.
  • Able to write, review and edit regulatory documentation, ensuring it is fit for purpose, and to serve as a resource for regulatory document authors regarding the appropriate content of submissions.
Person Spec
  • Minimum Bachelor’s degree; studies in science and advanced degree desirable
  • Minimum 10+ years progressive Regulatory Affairs or relevant experience
  • Specialized knowledge that would be desirable and supportive of success in this position includes:
    • Understanding of regulatory requirements for and experience with submission of applications (CTA/MAA) in eCTD format
    • Ability to create and manage detailed timelines and/or experience with tracking regulatory activities across disciplines and territories
    • Experience in other key functional areas, (e.g., toxicology, pharmacology, chemistry/manufacturing, clinical research and/or biometrics) appreciated
    • Experience with US and international management of post-marketing CMC changes
    • Experience in paediatric drug development and understanding of EU regulations related to paediatric requirements
  • Experience in the management of core labelling and/or EU labelling

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