Manager, Safety Analysis Scientist

Johnson & Johnson

. Lead safety evaluations, including strategy discussions, data retrieval, data analysis, report writing, and report revision .

Posted 9/29/2026full-timeUnited StatesSeniorLead💰 $117,000 - $201,250 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in safety evaluations, medical writing, and pharmacovigilance, with a strong ability to analyze complex medical data and prepare high-quality reports. Proven leadership in cross-functional team environments, ensuring compliance with global safety health authority requirements.

Highest-signal resume keywords

Medical WritingPharmacovigilanceSafety EvaluationsData AnalysisLeadership Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data RetrievalReport WritingSignal TrackingComplex Data InterpretationMedical Concept Knowledge

Soft Skills

Excellent Communication SkillsTeam CollaborationInfluencing SkillsNegotiation SkillsTime Management

Tools & Technologies

Microsoft WordMicrosoft ExcelMicrosoft PowerPoint

Industry Keywords

HealthcareBiomedical ScienceDrug DevelopmentPost-Marketing SafetyGlobal Safety Health Authority Requirements

About the role

Key responsibilities & impact

Lead safety evaluations, including strategy discussions, data retrieval, data analysis, report writing, and report revision
Collaborate with the Therapeutic Area Safety Head, Medical Safety Officer, and other team members
Ensure high-quality safety evaluations and reports with minimal-to-moderate comments and revisions
Provide support to Associate Director Safety Analysis Scientists on novel projects without defined processes
Provide input and review for key regulatory or clinical documents
Demonstrate leadership in the Safety Management Team and support the Medical Safety Officer
Prepare and present data, compile meeting minutes, and update signal tracking information
Lead proactive safety data reviews
Serve as the product point of contact and mentor team members on complex reports
Build cross-functional alliances to shape safety-related decisions and outcomes

Requirements

What you’ll need

Bachelor’s Degree required in Healthcare-related or Biomedical Science
9+ years industry experience or equivalent with a bachelor’s degree
Advanced degree preferred in Healthcare-related or Biomedical Science
6+ years industry experience or equivalent with an advanced degree
Medical writing or pharmacovigilance (PV) experience required
Clinical experience preferred
Working knowledge of medical concepts
Familiarity with safety activities in drug development and post-marketing
Familiarity with global safety health authority requirements
Ability to understand and analyze complex medical-scientific data from a broad range of sources
Ability to interpret and present complex data to determine benefit-risk impact
Excellent English verbal and written communication skills
Ability to effectively interact with team members and business partners
Ability to work in a cross-functional team environment
Proven leadership skills
Ability to plan work to meet timelines and balance multiple priorities
Proficiency in Microsoft Word, Excel, and PowerPoint
Ability to influence, negotiate, and connect with internal and external customers

Benefits

Comp & perks

Retirement plan (pension)
Savings plan (401(k))
Vacation – 120 hours per calendar year
Sick time – 40 hours per calendar year; 48 hours for employees residing in Colorado; 56 hours for employees residing in Washington
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 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
Inclusive interview process and accommodation support