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GLOBAL CLINICAL AFFAIRS MANAGER

24/12/2022

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​Vision Executives are experts in international recruitment for the eyecare industry and we have partnered with a global leader in ophthalmic medical devices who are looking for a Clinical Affairs Manager to drive the clinical evidence for refractive lasers and presbyopia treatment to support global regulatory approvals.
The company I am representing are one of the global market leaders in ophthalmology and are planning on launching new technology soon. For this Germany based role they are offering a market leading salary package and benefits.

If if this particular role does not interest you they are expanding rapidly and have positions available including; Clinical Study Manager, Clinical Applications Specialist, Clinical Data Manager & Regulatory Affairs. As such, please apply and we can keep you in mind for other upcoming positions.

We are looking for a person who can:
  • Responsible for budgeting and scheduling of overall clinical strategy
  • Review and approval of product-specific marketing materials and publications
  • Continuous collaboration in project teams for new and further product developments from product definition to market launch
  • Assisting Clinical/Regulatory Affairs teams worldwide with product registration
  • Participation in adapting and improving clinical affairs processes
  • Regular interdisciplinary and cross-site cooperation


You will need:
  • Ideally, a completed (technical) university degree in ophthalmology/optometry or medicine with a focus on ophthalmology
  • Alternatively scientific (technical) university studies (e.g. medical technology, biology, physics) or a comparable qualification
  • At least 3 years of relevant professional experience in the field of clinical affairs or clinical research in the medical technology industry or at contract research institutes
  • In-depth knowledge of the relevant regulatory requirements for clinical studies and evaluations for medical devices as well as experience and proven success in the design of clinical studies
  • Practical experience in project management and medical writing
  • Very good command of spoken and written English and German
  • Analytical skills and creativity as well as strong communication and organizational skills in an international environment
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