EMEA Regulatory Liaison

Job Ref: J25690
Sector: Clinical
Sub-sector: Pharmaceuticals
Date Added: 01 March 2018
  • High Wycombe, Buckinghamshire, England, UK
  • Competitive
  • Neal Panting
  • 01753 589601

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The role will be involved with day to day Regulatory Activities related to providing strategic input within Development, Post Approval and Life Cycle Management.Key Responsibilities/Requirements:* Provide advice on regulatory issues surrounding National and Centralised requirements, including devising and implementing Strategies. * Act as a primary point of contact with the EMEA with regards to Scientific Advice. Ensuring all responses are made in a timely manner.* Ensure CTA submission packages are completed and available to agreed timelines.* Manages submissions of MAA's, defines processes, submission plans and advise team on submissions strategies. Skills/Experience Required:* Bachelor's degree required or equivalent experience; Science degree or related experience with pharmaceutical or health sciences industry is required; knowledgeable with scientific terminology* Ideal candidate would possess a extensive experience within regulatory affairs in the pharmaceutical industry. An understanding of Drug Development, Clinical Trial Authorization Applications, Pips, Regulatory Affairs, and associated legal requirements is also required.* Strong working knowledge within Oncology/Haematology portfolios. If you are interested in this role or would like to have a confidential career discussion regarding other Regulatory Opportunities. Please contact me: or +441753 589626

The recruiter has stated that all applicants for this job should be able to prove they are legally entitled to work in the EU/UK. SRG is a trading name of Science Recruitment Group Ltd an Employment Business/Agency.