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Senior Manager, Bioethics, Policy & Partnerships
Johnson & Johnson. Provide project management support for the Bioethics, Policy & Partnerships team and selected Office of the Chief Medical Officer priorities .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates strong project management capabilities, including the development and management of integrated plans, timelines, and deliverables within a pharmaceutical or biotech environment. Possesses exceptional organizational skills, high emotional intelligence, and the ability to influence stakeholders and navigate complex team dynamics.
Highest-signal resume keywords
Project ManagementR&D ExperienceStakeholder EngagementRisk MitigationOrganizational Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Project ManagementIntegrated Plans DevelopmentTimeline ManagementMilestone TrackingRisk AssessmentDeliverable ManagementPolicy StewardshipWorkplan DevelopmentDocument ImplementationProduct Development
Soft Skills
Influencing Without AuthorityHigh Emotional IntelligenceInterpersonal SkillsCommunication SkillsAttention to Detail
Tools & Technologies
Status DashboardsAction LogsDecision LogsRisk RegistersVersion-Controlled Repositories
Industry Keywords
PharmaceuticalBiotechMedTechR&DComplianceEthical StandardsStakeholder ConsultationGovernance OperationsPolicy DevelopmentProduct Development Team
About the role
Key responsibilities & impact- Provide project management support for the Bioethics, Policy & Partnerships team and selected Office of the Chief Medical Officer priorities
- Partner with OCMO colleagues and external communications agencies to execute cross-OCMO communications strategy
- Coordinate internal employee communications, including town halls
- Develop and maintain OCMO communications plans with milestones, owners, dependencies, review cycles, and delivery dates
- Support implementation and execution of the OCMO Policy Stewardship process
- Build and manage policy stewardship workplans covering intake, assessment, stakeholder consultation, drafting, review, approval, implementation, and reassessment
- Coordinate stakeholder outreach and review cycles; consolidate comments; track feedback disposition; confirm issue resolution and approvals
- Maintain centralized trackers for policy owners, decision-makers, review dates, dependencies, risks, decisions, and implementation commitments
- Prepare status updates and governance materials highlighting progress, milestones, overdue actions, decision points, and escalation matters
- Lead or support project management assignments for BPP and OCMO priorities
- Translate strategic priorities into executable workplans with scope, roles, deliverables, success measures, and governance checkpoints
- Coordinate committee and governance operations, including agendas, pre-reads, meeting logistics, minutes, action tracking, and decision follow-up
- Facilitate project kickoffs and recurring status meetings
- Coordinate inputs and approvals across OCMO functions and agency partners; identify conflicts and escalate risks with mitigation options
- Maintain status dashboards, action logs, decision logs, risk and issue registers, and version-controlled repositories
- Conduct project closeouts and lessons-learned reviews; document outcomes and improve templates, tools, and ways of working
Requirements
What you’ll need- A Bachelor’s degree is required
- A minimum of 5 years of increasing business experience with a pharmaceutical/biotech/MedTech company is required
- Previous R&D/scientific experience required
- Ability to influence without authority, build alignment across functions, and facilitate teams to deliver outcomes
- Project management capability, including development and management of integrated plans, timelines, milestones, dependencies, risks, decisions, and deliverables
- Exceptional organizational skills and attention to detail
- Ability to manage multiple priorities and maintain accurate, timely follow-through
- High emotional intelligence, sound judgment, and well-developed interpersonal and communication skills
- Ability to navigate sensitive matters and diverse stakeholder perspectives
- Project management, exceptional organization and attention to detail, influencing without authority, and high emotional intelligence (EQ)
- Master’s degree in life sciences strongly preferred
- Ability to develop and implement work product/documents within an R&D setting strongly preferred
- Experience on a product development team highly preferred
- Track record of identifying, quantifying, and mitigating risk to meet ethical, legal, compliance, and business objectives preferred
Benefits
Comp & perks- Consolidated retirement plan (pension)
- Savings plan (401(k))
- Long-term incentive program
- Vacation – 120 hours per calendar year
- Sick time – 40 hours per calendar year; 48 hours for Colorado residents; 56 hours for Washington residents
- 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
- Equal opportunity and inclusive interview process
- Disability accommodation support