Medical Device Expert

11 hours ago


Stockholm, Stockholm, Sweden TN Sweden Full time
Key Responsibilities
  • Design and oversee clinical studies to meet regulatory and marketing requirements.
  • Collaborate with regulatory affairs teams to secure product approvals.
  • Develop and execute medical affairs strategies to support marketing efforts.
  • Assess and interpret scientific literature relevant to TN Sweden's products.

Requirements:

  • MD, PhD, PharmD, or similar advanced degree in a relevant field.
  • Previous experience in medical affairs, scientific communications, or clinical research.
  • Strong understanding of drug and medical device development and regulatory procedures.


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