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.


The selection, respects Legislative Decree 198/2006 and is open to candidates of any orientation or expression of gender, sexual orientation, age, ethnicity and religious belief. This announcement is designed to respect diversity and inclusiveness.

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