Pharmd Fellow Safety Analysis Scientist

Johnson & Johnson Johnson & Johnson · Pharma · Lisbon, Portugal

This role is a PharmD Fellow position focused on safety analysis and risk management within Johnson & Johnson's Innovative Medicine division. The fellow will prepare scientific safety analyses and evaluations for regulatory compliance and decision-making, support safety management teams, and gain experience in case processing and signal management. The role emphasizes collaboration, data analysis, and report writing in a healthcare/pharmaceutical context.

What you'd actually do

  1. Support safety evaluations, including strategy discussions, collaborating with Therapeutic Area Safety Head (TASH)/MSO and other stakeholders as necessary, data retrieval, data analysis, report writing, and report revision.
  2. With mentorship from the preceptor and/or Safety Analysis Scientist (SAS), ensure high quality safety evaluations and reports with moderate comments from stakeholders and moderate revisions required.
  3. Provide support to SAS for novel projects, to bring value through completion of task-based activities without defined processes.
  4. Support SMT activities (e.g. preparing and presenting data, compiling meeting minutes, updating signal tracking information).
  5. Provide support for Health Authority interactions regarding safety and risk management, both written and verbal.

Skills

Required

  • Doctor of Pharmacy degree
  • At least 2 years of industry experience or equivalent
  • Excellent English verbal and written communication skills
  • Ability to understand and analyze complex medical-scientific data from a broad range of sources
  • Ability to interpret and present complex data to determine benefit-risk impact
  • Ability to effectively interact with stakeholders, including business partners
  • Ability to work in a matrix environment, proven leadership skills
  • Ability to plan work to meet deadlines and effectively balance multiple priorities
  • Proficiency in Microsoft applications (e.g. Word, Excel, and PowerPoint)

Nice to have

  • Medical writing or pharmacovigilance experience
  • Solid understanding of medical concepts
  • Analytical Reasoning
  • Data Analysis
  • Data Reporting
  • Data Savvy
  • Researching
  • Safety Investigations
  • Serious Adverse Event Reporting
  • Technical Writing

What the JD emphasized

  • regulatory compliance