Healthcare Professional Specialist

2 days ago


Stockholm, Stockholm, Sweden PharmaRelations ApS Full time
Key Responsibilities:

The Clinical Affairs Specialist will be responsible for:

  1. Working closely with the Critical Care business area to design and coordinate CC sponsored clinical studies;
  2. Ensuring timely completion of studies and compliance with regulatory requirements;
  3. Managing and executing post-market clinical research studies and surveys;
  4. Maintaining up-to-date knowledge of regulatory requirements and guidelines;
  5. Collaborating with internal stakeholders to ensure smooth execution of clinical activities;
  6. Developing reports for submission to regulatory agencies as needed.

The ideal candidate will have a strong background in research and clinical studies, Good Clinical Practice, and ISO 14155 familiarity. Experience within the Medical Device industry and/or the life science industry is also required.



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