Role Description
The Senior Medical Director, Medical Science, is an experienced physician leader who provides strategic medical, scientific, and operational leadership across clinical development programs while serving as a trusted advisor to sponsors, investigators, and cross-functional teams. This role combines medical monitoring expertise with sponsor-facing leadership, business development support, and study oversight responsibilities.
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Serve as a senior medical and scientific leader in sponsor interactions, building trusted partnerships through proactive consultation, strategic insight, and exceptional service delivery.
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Represent the organization as the physician and subject matter expert during client meetings, scientific presentations, conferences, proposal discussions, and bid defense activities.
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Provide medical and scientific expertise during client feasibility assessments, including evaluation of study design, patient populations, enrollment strategies, and site selection.
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Serve as Medical Monitor for assigned studies, acting as the primary medical contact for sponsors, investigators, and study teams, providing medical oversight of patient safety.
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Review and interpret laboratory data, adverse events, medical coding dictionaries, and study data outputs, including tables, listings, and figures.
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Review and provide expert input into the Medical Monitoring Plan, study protocols, statistical analysis plans, case report forms, training materials, investigator brochures, clinical study reports, and other key study documents.
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Conduct independent medical analyses of emerging study data and effectively communicate findings, risks, and recommendations to sponsors and internal stakeholders.
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Collaborate with Safety/Pharmacovigilance teams to review safety documentation and support safety signal evaluation and risk management activities.
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Contribute medical expertise to safety review meetings, data monitoring activities, and governance committees as required.
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Lead complex global clinical programs and provide oversight and guidance to regional medical leaders and project teams, as appropriate.
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Participate in investigator meetings and scientific advisory discussions as the medical representative for assigned programs.
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Mentor, coach, and develop Medical Directors, Associate Medical Directors, and other colleagues across the organization.
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Identify opportunities to improve processes, efficiencies, quality, and client experience across Medical Sciences and the broader organization.
Qualifications
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MD, DO, MBBS or equivalent education with completion of residency in a medical or pediatric sub-specialty, including completion of a fellowship in hematology and/or oncology.
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At least 10 years combined experience in academic and/or industry clinical research in drug development.
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Experience as a Medical Monitor on clinical oncology and/or rare clinical trials is required.
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Clinical practice experience of a minimum of 3-5 years preferred.
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Board certification in hematology and/or oncology preferred.
Requirements
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Lead with integrity, professionalism, and transparency in all interactions.
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Anticipate client needs and provide innovative solutions that consistently meet or exceed expectations.
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Lead medical strategy and scientific discussions in both prepared and extemporaneous settings.
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Demonstrate accountability and ownership for outcomes, proactively identifying root causes of issues and implementing sustainable solutions.
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Model company values and foster a culture focused on patient care, scientific excellence, collaboration, and continuous improvement.
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Effective level of communication (both written and verbal) skills and effective level of salesmanship and presentation skills.
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Proficiency and sensitivity to work in a global company with reports from varied cultures and backgrounds.
Benefits
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Discretionary annual bonus.
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Health insurance.
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Retirement savings benefits.
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Life insurance and disability benefits.
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Parental leave.
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Paid time off for sick leave and vacation.