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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive expertise in Clinical Development and Clinical Science leadership, particularly in Genitourinary oncology, with a strong focus on clinical trial design, data interpretation, and cross-functional collaboration. Proven ability to manage and develop scientific teams while ensuring compliance with regulatory standards and promoting innovative practices.
Highest-signal resume keywords
Clinical DevelopmentClinical Research ManagementOncologyPeople LeadershipClinical Trial Planning
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical ScienceClinical Trial DesignData InterpretationStudy DesignTherapeutic KnowledgeRegulatory SubmissionsPortfolio DiscussionsCross-Program PlanningClinical Data ReviewBiomarker Strategy
Soft Skills
Excellent CommunicationInfluenceExecutive Presentation SkillsCoachingMentoring
Tools & Technologies
Visual AnalyticsAI-Enabled WorkflowsCentralized Data Review
Industry Keywords
Genitourinary CancersPharmaceutical IndustryBiotechnology IndustryClinical Drug DevelopmentHealth Authority Interactions
About the role
Key responsibilities & impact- Provide strategic Clinical Science leadership across multiple GU oncology studies, programs, and assets
- Contribute Clinical Science input to disease area strategy, development opportunities, portfolio risks, and emerging data assessment
- Partner with Section Heads, Asset Leads, Program Development Team Leads, and cross-functional leaders on study and program objectives
- Apply therapeutic expertise to study planning, data interpretation, issue resolution, and development strategy
- Standardize Clinical Science approaches, medical data review practices, data interpretation principles, and key deliverables
- Promote consistency and establish leading practices across studies and programs
- Advocate for visual analytics, centralized data review, AI-enabled workflows, and other efficiency technologies
- Guide interpretation of clinical data across studies, cohorts, and assets
- Support protocol development, amendments, study design, endpoint selection, eligibility criteria, and biomarker strategy
- Serve as a Clinical Science subject matter resource for GU oncology
- Contribute to portfolio discussions, governance reviews, senior leadership meetings, and program reviews
- Prepare and present clinical and scientific content, assessments, cross-study insights, and key issues
- Translate portfolio priorities into Clinical Science strategies, capabilities, and resource plans
- Directly manage Directors, Principal Scientists, and Clinical Scientists as appropriate
- Set expectations and develop talent through coaching, mentoring, feedback, and development opportunities
- Foster accountability, inclusion, continuous learning, and strong team performance
- Partner with Clinical Operations, Regulatory Affairs, Biostatistics, Data Management, Drug Safety and Pharmacovigilance, Translational Medicine, Medical Affairs, and other functions
- Represent Clinical Science in cross-functional planning and strategic decision-making forums
- Ensure compliance with regulatory requirements, company policies, and established procedures
- Support inspection readiness and documentation
- Identify opportunities to improve Clinical Science quality, consistency, and effectiveness
- Maintain awareness of relevant scientific, clinical, and regulatory developments
Requirements
What you’ll need- Advanced scientific or healthcare degree required (e.g., PhD, PharmD), or equivalent, with 8+ years of pharmaceutical, clinical drug development, and/or medical field experience preferred
- OR Master’s degree, preferably in life sciences, with 12+ years of pharmaceutical, clinical drug development, and/or medical field experience
- OR Bachelor’s degree, preferably in life sciences, with 15+ years of pharmaceutical, clinical drug development, and/or medical field experience
- Significant experience in Clinical Development, Clinical Science, clinical drug development, or a related function within the pharmaceutical or biotechnology industry
- Demonstrated Clinical Science leadership across multiple studies, programs, or assets
- Deep therapeutic area expertise in Genitourinary cancers, including disease biology, treatment landscape, clinically relevant endpoints, and development considerations
- Strong understanding of clinical trial design, clinical development strategy, clinical data review, and interpretation of oncology data
- Experience contributing to disease area strategy, portfolio discussions, or cross-program planning
- Experience contributing to regulatory submissions, safety reviews, or health authority interactions
- Experience working effectively in cross-functional teams within a matrix environment
- Ability to integrate information across studies and programs to support scientific and business decisions
- Excellent communication, influence, and executive presentation skills
- Demonstrated people leadership experience, including management, coaching, and development of scientific staff
- Required skills: Clinical Development, Clinical Research, Clinical Research Management, Clinical Sciences, Clinical Trial Planning, Oncology, People Leadership, Study Design, Therapeutic Knowledge, Trial Design
- No visa sponsorship
Benefits
Comp & perks- Annual bonus eligibility
- Long-term incentive, if applicable
- Medical, dental, and vision healthcare benefits for employee and family
- Other insurance benefits for employee and family
- Retirement benefits, including 401(k)
- Paid holidays
- Vacation
- Compassionate and sick days
- Hybrid work arrangement
- 10% travel requirement
- No relocation required