Manager, Safety Analysis Scientist

Scorpion Therapeutics; Horsham (PA); On-site; USD 120,000 - 180,000; Full time

Job summary

Johnson & Johnson's Innovative Medicine division seeks a Manager, Safety Analysis Scientist to lead scientific safety assessments of pharmaceutical products. You will manage safety data reviews and contribute to benefit-risk analyses for developmental and marketed drugs.

Required background in pharmacovigilance or clinical safety with strong medical writing skills and knowledge of global regulatory standards; mentoring and cross-functional collaboration are valued.

Qualifications

• Bachelor's in Healthcare or Biomedical Science with 9+ years of industry experience.
• Advanced degrees preferred with 6+ years.
• Background in pharmacovigilance, medical writing, or clinical safety required.
• Knowledge of drug development safety activities and global regulatory standards essential.

Responsibilities

• Lead safety data reviews.
• Develop and revise safety reports.
• Collaborate with Medical Safety Officers and cross-functional teams.
• Support regulatory documentation.
• Mentor team members on complex safety reports.

Skills

Medical data interpretation

Scientific communication

Cross-functional collaboration

Project planning

Microsoft Office

Education

Bachelor's in Healthcare or Biomedical Science

Advanced degrees preferred

Tools

Microsoft Office

Job description

Role

Manager, Safety Analysis Scientist responsible for scientific safety assessments of pharmaceutical products within Johnson & Johnson's Innovative Medicine division.

Objectives

provide expert safety evaluations, support regulatory compliance, and contribute to benefit-risk analyses for marketed and developmental drugs.

Responsibilities

• lead safety data reviews
• develop and revise safety reports
• collaborate with Medical Safety Officers and cross-functional teams
• support regulatory documentation
• mentor team members on complex safety reports

Qualifications

• Bachelor's in Healthcare or Biomedical Science with 9+ years industry experience
• advanced degrees preferred with 6+ years
• background in pharmacovigilance, medical writing, or clinical safety required
• knowledge of drug development safety activities and global regulatory standards essential

Skills

strong medical data interpretation, scientific communication, cross-functional collaboration, project planning, and proficiency in Microsoft Office.

Experience

Experience in clinical safety, post-marketing surveillance, and global safety regulations is highly valued.

Location options

Location options include Horsham, PA, and Raritan/Titusville, NJ, with no specific travel mentioned.