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Senior Director, Translational Research
Verastem Oncology. Lead the development and execution of biomarker and pharmacodynamic strategies for Verastem clinical studies .
Posted 9/24/2026full-timeNeedham • Massachusetts • United StatesSenior💰 $210,000 - $265,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Expertise in biomarker and pharmacodynamic strategies for oncology clinical studies, with a strong foundation in cancer biology and translational research methodologies. Proven ability to analyze complex biological datasets and communicate findings effectively across multidisciplinary teams.
Highest-signal resume keywords
Ph.D. In Cancer BiologyBiomarker ResearchTranslational ResearchProject ManagementScientific Communication
ATS Keywords
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Hard Skills
Oncogenic Signaling PathwaysTumor DependenciesPharmacodynamic AnalysesHypothesis-Driven ResearchData AnalysisClinical Biospecimen WorkflowsBiomarker AssaysBioinformaticsTranslational Hypotheses GenerationRegulatory Submissions
Soft Skills
CollaborationOrganizational SkillsCommunication Skills
Industry Keywords
Clinical StudiesPharmacodynamicsBiotechnologyCancer ResearchExternal Vendors
About the role
Key responsibilities & impact- Lead the development and execution of biomarker and pharmacodynamic strategies for Verastem clinical studies
- Collaborate with preclinical research colleagues to design and execute translational studies using in vitro and in vivo models
- Inform indication selection, pharmacodynamic biomarkers, patient-selection strategies, and rational drug combinations
- Analyze, interpret, and present clinical and translational biomarker data to identify biological insights and support clinical development decisions
- Integrate biomarker findings with clinical, molecular, and preclinical data to generate and evaluate translational hypotheses
- Oversee external vendors responsible for biospecimen storage, biomarker assays, bioinformatics analyses, and associated databases
- Review scientific literature, emerging datasets, and the competitive landscape, and participate in relevant scientific conferences
- Contribute to regulatory submissions, study reports, manuscripts, abstracts, posters, and scientific presentations
- Communicate findings and coordinate activities across cross-functional teams and external research partners
Requirements
What you’ll need- Ph.D. in cancer biology, molecular biology, cell biology, pharmacology, biochemistry, immunology, or a related discipline, with at least 12 years of relevant industry research experience in oncology; or an equivalent combination of education and experience
- Strong understanding of cancer biology, oncogenic signaling pathways, tumor dependencies, and mechanisms of therapeutic response and resistance
- Experience with biomarker research, pharmacodynamic analyses, and/or translational research supporting oncology drug development is highly desirable
- Familiarity with clinical biospecimen workflows and external biomarker vendors is preferred
- Demonstrated ability to design, execute, analyze, and interpret hypothesis-driven translational research
- Experience analyzing and interpreting complex biological datasets and translating results into actionable hypotheses
- Excellent written, verbal, and scientific communication skills, including the ability to communicate complex findings clearly to multidisciplinary audiences
- Demonstrated ability to collaborate effectively as part of cross-functional teams and with external partners
- Strong organizational and project-management skills with the ability to manage multiple priorities and timelines
- Ability to thrive in a fast-paced, highly collaborative biotechnology environment
Benefits
Comp & perks- Annual bonus eligibility
- Equity compensation
- Competitive benefits package