Regulatory Affairs Specialist

1 month ago

Central London, United Kingdom Pharmiweb Full time
Regulatory Affairs Consultant

Parexel Consulting is seeking a skilled and experienced CMC Regulatory Affairs Professional to join our team as a Regulatory Affairs Consultant. In this role, you will have the opportunity to utilize your expertise in CMC, exceptional communication skills, and strong writing experience, contributing to our clients' success in the pharmaceutical industry.

Key Responsibilities:
  • Assisting in the technical review and preparation of investigational drug applications, marketing applications, and other reports for submission to regulatory agencies.
  • Ensuring that documents meet established regulatory requirements in terms of content and structure.
  • Serving as a liaison between various functional groups, program teams, international regulatory bodies, and business partners, proposing solutions based on your technical experience and identifying potential project timeline delays.
  • Maintaining Regulatory CMC documentation.
  • Managing related databases and submission schedules.
  • Assisting in the development of submission plans and project timelines.
  • Preparing for and interacting with regulatory agencies during drug submissions, responding to inquiries, and participating in regulatory agency inspections.
Requirements:
  • University degree in a scientific field.
  • At least 5 years of relevant experience in the pharmaceutical industry or a regulatory authority.
  • Successful experience in delivering CMC sections of marketing authorizations, investigational drugs, and life cycle management of commercial products.
  • Knowledge of EMA guidance, regulations, and ICH/GMP requirements.
  • Previous regulatory experience with small molecule.
  • Experience with EU submissions via the Centralised Procedure and national procedures.
  • Experience with extension applications for new strengths and/or pharmaceutical dosage forms.
  • Experience supporting the preparation of CMC documentation for IMPDs and new product EU MAAs would be advantageous.
  • Ability to work independently and within project teams or committees, demonstrating accountability in achieving group goals and key project milestones.
  • Fluent in English written and spoken.

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