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Medical Safety Officer, Immunology
Johnson & JohnsonMedical Safety Officer assessing the medical safety of Innovative Medicine products with cross-functional team responsibilities at Johnson & Johnson. Leading safety management and risk assessment activities in a collaborative environment.
Posted 7/10/2026full-timeHorsham • New Jersey, Pennsylvania • 🇺🇸 United StatesJuniorMid-LevelWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in assessing medical safety and risk mitigation strategies for Innovative Medicine products, with a strong foundation in pharmacovigilance and clinical medicine. Proven ability to lead cross-functional teams and communicate effectively with stakeholders regarding safety data and clinical protocols.
Highest-signal resume keywords
Physician (MD Or Equivalent)Pharmacovigilance ExperienceClinical Medicine SkillsKnowledge Of Drug Development PrinciplesHealth Authority Presentation Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Risk Mitigation StrategiesSafety Data AssessmentClinical Protocol DesignSafety Management LeadershipMedical Expertise
Soft Skills
Influencing StakeholdersEffective Communication
Certifications & Qualifications
Board CertifiedBoard Eligible
Industry Keywords
Global Safety RegulationsClinical Practice ExperienceCross-Functional Team Leadership
About the role
Key responsibilities & impact- Assess the medical safety of Innovative Medicine products
- Strategically lead cross-functional matrix teams
- Ensure proactive and timely assessments of safety data
- Communicate potential and known risks to relevant stakeholders
- Design and implement risk mitigation strategies
- Provide medical and scientific expertise on various teams
- Influence design of clinical protocols to minimize patient impact
- Lead Safety Management Teams for assigned products
Requirements
What you’ll need- Physician (MD or equivalent)
- 2-5 years of pharmacovigilance (PV) experience or other relevant experience
- Board Certified/Board Eligible/equivalent preferred
- Demonstrated skills in clinical medicine with at least 1 year of clinical practice experience
- Demonstrated knowledge of principles of drug development and global safety regulations highly preferred
- Ability to influence and communicate with stakeholders
- Experience with Health Authority presentations preferred
Benefits
Comp & perks- Inclusive work environment
- Opportunities for professional development