PharmD Fellow, Safety Analysis Scientist

Scorpion Therapeutics

Horsham (PA)

On-site

USD 90,000 - 120,000

Full time

8 days ago
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Job summary

Johnson & Johnson is seeking a PharmD Fellow, Safety Analysis Scientist in Product Safety Risk Management at its Horsham, PA location. The role focuses on safety analyses and regulatory compliance for innovative medicines, with responsibilities across safety evaluations, data analysis, and report writing.

The Fellow will collaborate cross-functionally, support novel projects, participate in rotational safety activities, and assist in program development and precept pharmacy students.

Qualifications

  • PharmD degree (or recent ACPE-accredited graduate).
  • Strong medical concept understanding.
  • Excellent communication skills.
  • Ability to analyze complex data.
  • Proficiency in Microsoft Office.
  • Experience in safety or clinical operations preferred.

Responsibilities

  • Support safety evaluations.
  • Data retrieval and analysis.
  • Report writing.
  • Contribute to safety management team activities.
  • Assist with health authority interactions.
  • Rotate through safety activities like case processing and signal management.
  • Assist in program development and precept pharmacy students.

Skills

Data analysis
Communication
Regulatory knowledge
Safety operations
MS Office

Education

PharmD degree
ACPE-accredited program

Tools

Microsoft Office

Job description

Role: PharmD Fellow, Safety Analysis Scientist in Product Safety Risk Management at Johnson & Johnson, focusing on safety analyses and regulatory compliance for innovative medicines.

Responsibilities
  • support safety evaluations
  • data retrieval and analysis
  • report writing
  • contribute to safety management team activities
  • assist with health authority interactions

The role involves preparing safety evaluations, collaborating cross-functionally, supporting novel projects, and participating in rotational safety activities like case processing and signal management. The Fellow will also assist in program development and precept pharmacy students.

Requirements
  • PharmD degree (or recent graduate from an ACPE-accredited program)
  • strong medical concept understanding
  • excellent communication skills
  • ability to analyze complex data
  • proficiency in Microsoft Office
  • experience in safety or clinical operations preferred
HighValue
  • postdoctoral safety analysis
  • regulatory interactions
  • safety evaluations
  • medical data interpretation
  • cross-functional collaboration in innovative medicine
  • with potential exposure to clinical trial safety data and risk management strategies
WorkSetup

location in Horsham, PA, with responsibilities supporting global safety strategies.

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