Manager, Safety Analysis Scientist

Scorpion Therapeutics; Raritan (NJ); Hybrid; USD 140,000 - 210,000; Full time

Job summary

Johnson & Johnson's Product Safety Risk Management team is seeking a Manager, Safety Analysis Scientist to lead safety evaluations, data analysis, and report writing for innovative medicines. You will collaborate with Medical Safety Officers and cross-functional teams, support regulatory compliance and safety decisions, mentor staff, and contribute to safety data reviews and regulatory input.

Located in PA or NJ with remote/hybrid options, the role emphasizes cross-functional stakeholder

Qualifications

• Bachelor's degree in healthcare or biomedical sciences with 9+ years industry experience, or advanced degree with 6+ years.
• Experience in medical writing, pharmacovigilance, or clinical safety.
• Strong knowledge of safety activities in drug development and post-marketing.
• Skilled in analyzing complex medical data and interpreting benefit-risk profiles.
• Proficient in Microsoft Office.
• Excellent communication and cross-team collaboration skills.

Responsibilities

• Lead safety evaluations, data analysis, and report writing
• Collaborate with cross-functional teams including Medical Safety Officers
• Support regulatory compliance and safety decisions
• Mentor team members
• Support safety data reviews and regulatory document input

Skills

Cross-functional collaboration

Medical writing

Pharmacovigilance

Clinical safety

Education

Bachelor's degree in healthcare or biomedical sciences

Advanced degree (MS/PhD)

Tools

Microsoft Office

Job description

Role

Manager, Safety Analysis Scientist within Johnson & Johnson's Product Safety Risk Management team, focusing on safety assessment of innovative medicines.

Responsibilities

• Lead safety evaluations, data analysis, and report writing
• Collaborate with cross-functional teams including Medical Safety Officers
• Support regulatory compliance and safety decisions
• Mentor team members
• Support safety data reviews and regulatory document input

Requirements

• Bachelor's degree in healthcare or biomedical sciences with 9+ years industry experience, or advanced degree with 6+ years
• Experience in medical writing, pharmacovigilance, or clinical safety
• Strong knowledge of safety activities in drug development and post-marketing
• Skilled in analyzing complex medical data and interpreting benefit-risk profiles
• Proficient in Microsoft Office
• Excellent communication and cross-team collaboration skills

Preferred

• Clinical experience and familiarity with global safety regulations

HighValue

Focus on Innovative Medicine, safety assessment of marketed and in-development pharmaceuticals, supporting regulatory compliance, cross-functional stakeholder interaction, located in PA or NJ, remote/hybrid options.