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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in developing non-clinical safety strategies and integrating them with regulatory and clinical plans to enhance drug development. Proven ability to lead multidisciplinary teams, influence stakeholders, and mentor project members in a global environment.
Highest-signal resume keywords
Non-Clinical Safety ExpertiseProject Management Across Multiple ProjectsRegulatory Requirements KnowledgeToxicology ExperienceDABT Certification
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Non-Clinical SafetyToxicologyDrug DevelopmentProject Team CollaborationMarket ResearchCompetitive IntelligenceData IntegrationRegulatory DocumentationLong-Acting Small MoleculesInfectious Disease Therapy
Soft Skills
CoachingMentoringInfluencing StakeholdersPrioritizationCollaboration
Certifications & Qualifications
DABT
Industry Keywords
Drug DispositionOn-Target EngagementOff-Target ModulationPre-Clinical SafetyBiologics
About the role
Key responsibilities & impact- Develop end-to-end non-clinical safety strategies for projects across ViiV Healthcare’s portfolio
- Collaborate in a highly matrixed global environment
- Evolve non-clinical safety strategies using market research, competitive intelligence, and internal program learnings
- Integrate non-clinical project plans with CMC, regulatory, and clinical plans to optimize drug-development speed
- Serve as a toxicology project team member supporting 5–10 projects at a time
- Drive project activities in discovery and development phases, including external diligence
- Contribute to multidisciplinary scientific and operational strategies
- Integrate data and craft narratives for internal governance reviews and regulatory documentation
- Influence external stakeholders, including regulators, and senior ViiV/GSK leaders
- Coach and mentor project team members and review or approve regulatory and internal milestone documents
- Lead major scientific or technical initiatives
- Prioritize conflicting objectives and provide options to project teams and leadership
- Collaborate with GSK pre-clinical sciences and academic institutions
- Participate in due diligence teams evaluating external opportunities
- Provide consultancy on drug disposition, pre-clinical safety, and on-target/off-target engagement or modulation
- Contribute to toxicologist training and mentoring
- Participate in internal and external committees and panels
Requirements
What you’ll need- Master’s degree with 8+ years of experience in non-clinical safety/toxicology, or PhD with 6+ years of experience in non-clinical safety/toxicology
- Experience as a project team member covering multiple projects across a broad range of development stages and modalities, including biologics
- Non-clinical Safety capability and experience
- Understanding of the interrelationships between disposition, safety, and on/off-target engagement
- Knowledge and experience of worldwide regulatory requirements for drug development and registration
- Experience in non-clinical discovery and development of long-acting small molecules (preferred)
- DABT (Diplomat of American Board of Toxicology) (preferred)
- Experience in infectious disease therapy area (preferred)
- May be a recognized leader in a specific scientific field or discipline, with an extensive network and publication record (preferred)
Benefits
Comp & perks- Annual bonus
- Eligibility to participate in share-based long-term incentive program
- Health care benefits for employee and family
- Other insurance benefits for employee and family
- Retirement benefits
- Paid holidays
- Vacation
- Paid caregiver/parental leave
- Paid medical leave
- Domestic relocation package
- Accommodation or other assistance to apply, if required