1. Master’s Degree in Pharmaceutical Chemistry, Pharmacy, Medicines or Biology.
  2. Experience in preparing documents to meet the evolving needs of Health Authorities using expertise in writing, science and regulatory requirements.
  3. Global understanding of EU/USA regulatory requirements.
  4. Experience in global drug development projects bringing novel pharmaceutical products to market through planning and preparing a broad range of clinical and safety regulatory documents.
  5. Good written and oral communication skills in English.
  6. Willing to travel to on-site projects as required.

Comments are closed for this post.