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Associate Director – Medical Safety Officer, Oncology
Johnson & JohnsonAssociate Medical Safety Officer leading product safety and benefit-risk assessments for Janssen in oncology. Collaborating with cross-functional teams to manage safety profiles and risk management strategies.
Posted 7/23/2026full-timeHorsham • New Jersey, Pennsylvania • 🇺🇸 United StatesSenior💰 $159,000 - $274,850 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Clinical Operations and Risk Management while leading Safety Management Teams to assess the medical safety of products. Collaborates effectively across functions to influence safety strategies and ensure compliance with regulatory standards.
Highest-signal resume keywords
Clinical OperationsRisk ManagementSafety InvestigationsCross-Functional CollaborationSerious Adverse Event Reporting
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Compliance ManagementQuality ControlResearch EthicsStandard Operating ProcedureTactical Planning
Soft Skills
Developing OthersTeam ManagementTechnical Credibility
Industry Keywords
Medicines DevelopmentDevice DevelopmentPatient Risk ManagementSafety Management TeamsBenefit-Risk Balance
About the role
Key responsibilities & impact- Assessing the medical safety of assigned Janssen products
- Work closely with experienced Medical Safety Officer to lead cross-functional matrix teams
- Execute on the Global Medical Safety organization’s strategy
- Serve as a subject matter expert in the therapeutic area and patient risk management
- Lead the Safety Management Teams (SMT) for assigned products
- Build collaborative partnerships with other GMS groups and functional stakeholders
- Provide medical and scientific expertise as the GMS representative
- Anticipate safety concerns and influence relevant functions
- Assess product benefit-risk balance and provide input
Requirements
What you’ll need- Experience in Clinical Operations, Compliance Management, Compliance Risk, Cross-Functional Collaboration, Developing Others, Medicines and Device Development and Regulation, Quality Control (QC), Research Ethics, Risk Management, Safety Investigations, Serious Adverse Event Reporting, Standard Operating Procedure (SOP), Surveillance, Tactical Planning, Team Management, Technical Credibility.
Benefits
Comp & perks- Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
- This position is eligible to participate in the Company’s long-term incentive program.
- Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
- Vacation –120 hours per calendar year
- Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
- Holiday pay, including Floating Holidays –13 days per calendar year
- Work, Personal and Family Time - up to 40 hours per calendar year
- Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
- Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
- Caregiver Leave – 80 hours in a 52-week rolling period
- Volunteer Leave – 32 hours per calendar year
- Military Spouse Time-Off – 80 hours per calendar year