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Scientific Director
GSKScientific Director leading safety evaluation and risk management for GSK oncology assets. Collaborating cross-functionally to ensure robust assessment and communication of safety risks.
Posted 7/7/2026full-timeMassachusetts, Pennsylvania • 🇺🇸 United StatesLead💰 $169,950 - $283,250 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates advanced expertise in safety evaluation and risk management within oncology clinical development, with a strong focus on pharmacovigilance and drug safety. Capable of leading cross-functional teams to address complex safety issues and ensure compliance with global pharmacovigilance requirements.
Highest-signal resume keywords
PharmacovigilanceRisk ManagementSignal DetectionSafety SurveillanceClinical Development
ATS Keywords
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Hard Skills
Safety EvaluationRisk AssessmentClinical Data InterpretationBenefit-Risk Profile AnalysisDrug Development Processes
Soft Skills
Cross-Functional CollaborationCommunicationDecision-MakingJudgment
Industry Keywords
OncologyPharmaceutical IndustryBiotech IndustryPost-Marketing SurveillanceSafety Review Team
About the role
Key responsibilities & impact- Provides advanced scientific expertise in the safety evaluation and risk management of key GSK oncology assets in clinical development.
- Leads the identification, assessment, and communication of safety risks to ensure robust benefit-risk profiles and protection of patients globally.
- Partners cross-functionally to ensure high-quality, timely decision-making and proactive risk mitigation across the portfolio.
- Represent Safety Evaluation & Risk Management (SERM) on Clinical Matrix and Project Teams.
- Lead cross-functional efforts to address urgent and complex product safety issues.
- Prepare and present at Safety Review Team (SRT) meetings.
Requirements
What you’ll need- Degree in a health or life sciences discipline (e.g., Bachelor of Science, PharmD, MD, PhD, or equivalent).
- Minimum 5 years experience in pharmacovigilance, drug safety, or related safety evaluation role in the pharmaceutical or biotech industry.
- Practical experience in signal detection, safety surveillance and risk management across clinical development and post-marketing.
- Knowledge of global pharmacovigilance requirements and drug development processes.
- Strong clinical or scientific judgement with experience interpreting clinical and safety data.
Benefits
Comp & perks- health care and other insurance benefits (for employee and family)
- retirement benefits
- paid holidays
- vacation
- paid caregiver/parental and medical leave