Verastem Oncology

Medical Director

• Establish and lead the global Medical Affairs vision and strategy
• Provide executive leadership for the Medical Affairs organization, including MSLs, Medical Communications, Publications, Medical Education, and Medical Information
• Serve as senior medical leader and strategic advisor to executive leadership and cross-functional partners
• Provide clinical and scientific guidance across Commercial, Market Access, Regulatory Affairs, Research & Development, Manufacturing, Legal, and Corporate Strategy
• Build and oversee relationships with KOLs, clinical investigators, scientific advisors, patient advocacy organizations, and professional societies
• Lead external scientific engagement, medical advisory boards, investigator meetings, medical congresses, scientific exchange, and executive presentations
• Partner with Commercial leadership on compliant medical education, field training, and promotional support materials
• Oversee the Investigator-Sponsored Trial strategy and governance process
• Drive scientific evidence generation and dissemination through publications, congress activities, real-world evidence, and collaborative research
• Ensure Medical Affairs compliance with regulatory requirements, industry standards, and corporate policies
• Recruit, develop, and mentor the Medical Affairs leadership team
• Represent Medical Affairs on the executive leadership team and contribute to corporate strategy, portfolio planning, business development evaluations, and organizational growth

Translator

• 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

Senior Director, Translational Research

Director

• Lead statistical work for one or more clinical studies within a clinical program
• Coordinate assigned statistical work and collaborate with programming staff
• Formulate and carry out statistical analyses of clinical trial data
• Communicate interpretation of results cross-functionally
• Support regulatory submissions and interactions, including responses to regulatory requests
• Author and review protocol sections on statistical methods, endpoints, objectives, and assessments
• Author or oversee statistical analysis plans and integrated summaries
• Author or edit shells for tables, figures, and listings
• Provide statistical input to data monitoring committee charters, project management plans, and other study-level documents
• Manage timelines for assigned statistical deliverables
• Conduct statistical modeling to support study designs and address statistical issues
• Review case report form designs
• Support ongoing safety review and independent data monitoring committee review
• Perform ad hoc and exploratory statistical analyses
• Contribute to clinical study reports, including statistical sections and interpretation of results
• Support preparation of publications, including manuscripts, posters, and oral presentations
• Oversee CROs performing outsourced statistical activities and quality-control key CRO-generated results
• Communicate complex statistical concepts and analysis results to cross-functional study teams

Associate Director – Biostatistics

Medical Science Liaison

• Serve as the field-based medical/scientific expert for Verastem Oncology
• Engage healthcare providers and provide fair/balanced education on investigational products and disease areas
• Establish and maintain collaborative relationships with investigators, institutions, groups, and consortia
• Increase company visibility and interact with current and future oncology leaders
• Participate in medical education for healthcare professionals, including formulary committees
• Ensure required education and training are provided at clinical sites
• Identify clinical research opportunities aligned with company objectives
• Serve as primary territory contact for investigator-initiated research from concept submission through publication
• Communicate clinical and research insights to shape company research
• Maintain clinical and scientific expertise through training, conferences, workshops, and publications
• Gather and disseminate compliant competitive intelligence
• Mentor MSL team members and contribute to the cross-functional Medical Affairs team
• Execute administrative aspects of regional field activities
• Provide medical leadership for internal cross-functional programs and projects
• Respond to unsolicited medical information requests
• Complete timely reports, project plans, and required documentation
• Senior MSL: contribute to publication planning, slide-deck development, training initiatives, and Medical Strategy Plan implementation
• Senior MSL: lead national priority projects, cross-functional initiatives, and selected external collaborations
• Senior MSL: mentor or coach other MSLs and coordinate advanced training initiatives

Medical Science Liaison, Senior Medical Science Liaison

• Serve as a biostatistics leader and manage statistical efforts for multiple clinical studies across a clinical program
• Provide leadership and guidance to biostatistics and statistical programming team members
• Formulate, carry out, and oversee statistical analyses of clinical trial data
• Communicate interpretation of results cross-functionally
• Lead regulatory submissions and independently respond to regulatory requests
• Author protocol statistical methods sections and review endpoints, objectives, and assessments
• Author or oversee statistical analysis plans and author/edit table, figure, and listing shells
• Provide statistical input to IDMC and IRC charters, project management plans, and other study-level documents
• Create and manage timelines for SAPs, analysis specifications, and IDMC documents
• Conduct statistical modeling for study design and statistical issues
• Review CRF designs and approve programming specifications for SDTM, ADaM, TLFs, and ad-hoc analyses
• Support ongoing safety and IDMC reviews
• Perform ad hoc and exploratory statistical analyses
• Contribute to clinical study reports and author statistical sections
• Support publications including manuscripts, posters, and oral presentations
• Oversee CROs and QC key results from outsourced statistical activities

Medical Director

Senior Director, Translational Research

Associate Director – Biostatistics

Medical Science Liaison, Senior Medical Science Liaison

Senior Director, Biostatistics