PharmD Fellow – Safety Analysis Scientist

About the role

The Global Safety Strategy & Risk Management (GSSRM) team at Johnson & Johnson is seeking a Pharm.D. Fellow to join its Safety Analysis function in Lisbon. This fellowship provides hands‑on training in safety data evaluation, regulatory reporting, and cross‑functional collaboration for marketed and pipeline products.

Key responsibilities

• Support safety evaluations, including strategy discussions, data retrieval, analysis, and report writing.
• Prepare scientific safety analyses and regulatory compliance documents under mentorship.
• Collaborate with Therapeutic Area Safety Heads, Medical Safety Officers, and Safety Management Teams.
• Assist in novel safety projects and task‑based activities without defined processes.
• Participate in safety data review meetings and contribute recommendations for product safety strategies.

Required profile

• Pharm.D. degree (or equivalent) with interest in drug safety and regulatory affairs.
• Strong scientific writing and analytical abilities.
• Willingness to work under guidance of a preceptor and Safety Analysis Scientist.
• Ability to interpret clinical trial data, medical literature, and safety surveillance information.

Required skills

• Scientific safety analysis
• Regulatory compliance documentation
• Data interpretation and report preparation