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Medical Expert

2 months ago

Hemel Hempstead, Hertfordshire, United Kingdom Merz Aesthetics UK and Ireland Full time
About the Role

We are seeking a highly skilled Scientific Advisor to join our team at Merz Aesthetics UK and Ireland. As a key member of our scientific services team, you will play a critical role in providing internal and external scientific support to ensure the needs of our customers and patients are met.

Key Responsibilities
  • Scientific Services
    • Provide scientific expertise to support the development and implementation of our aesthetic medicine portfolio.
    • Collaborate with cross-functional teams to ensure compliance with regulatory requirements and industry standards.
  • Compliance and Governance
    • Lead on compliance and governance initiatives to ensure Merz Aesthetics maintains high standards in all areas of the business.
    • Develop and implement policies and procedures to ensure adherence to regulatory requirements and industry standards.
  • Medical Support
    • Plan and execute medical support for our aesthetic medicine portfolio.
    • Identify and investigate new healthcare professionals to support our business growth.
  • Therapy Insights
    • Provide therapy insights to drive strategic business growth.
    • Develop and implement strategies to support the use of our products by healthcare professionals.
  • Medical Resources and Activities
    • Develop and lead the development of medical resources and activities to ensure they are fair, balanced, and compliant.
    • Collaborate with cross-functional teams to ensure alignment on content and compliance.
  • Research and Development
    • Support the Merz research program and life cycle management to identify unmet needs and build evidence and understanding for existing and potential therapeutic indications.
    • Collaborate with global teams to align on research and global medical projects.
Requirements
  • Qualifications
    • Graduate with a life-science qualification.
  • Experience
    • Experience in the pharmaceutical industry and copy approval.
    • Proven project management skills.
    • Analytical skills with the ability to understand and simplify complex medical messages.
    • Ability to communicate with impact.
  • Desirable
    • Registered Pharmacist/Physician with Medical final signatory status.
    • A strong understanding of PMCPA and medical governance.
    • Proven track record in developing and delivering medical education programmes.
    • Experience with clinical trials, Good Clinical Practice, and/or experience with managing CROs and/or local clinical trial sites.
  • Competencies
    • Teamworking.
    • Passion for Results.
    • Personal Accountability.
    • Open and Transparent.
    • Developing Self and Others.
    • Innovation.