Senior Medical Director – Oncology

Precision Medicine Group

. Serve as a senior medical and scientific leader in sponsor interactions .

Posted 10/28/2026full-timeRemote • United StatesSenior💰 $254,900 - $382,300 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive medical and scientific expertise in clinical research, particularly in oncology and hematology, with a strong focus on patient safety, operational excellence, and effective communication across diverse teams and cultures.

Highest-signal resume keywords

Medical Monitor ExperienceClinical Research ExpertiseOncology FellowshipBoard Certification in HematologyEffective Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial DesignData AnalysisMedical OversightAdverse Event ReviewStatistical AnalysisStudy Protocol DevelopmentMedical Monitoring PlansLaboratory Data InterpretationRisk ManagementPatient Safety Oversight

Soft Skills

LeadershipMentoringSalesmanshipPresentation SkillsCollaboration

Certifications & Qualifications

MDDOMBBSBoard Certification in HematologyBoard Certification in Oncology

Industry Keywords

Clinical ResearchDrug DevelopmentPharmacovigilanceGlobal Clinical ProgramsStudy Feasibility AssessmentsClinical Oncology TrialsRare Clinical TrialsScientific PresentationsClient InteractionsOperational Effectiveness

About the role

Key responsibilities & impact

Serve as a senior medical and scientific leader in sponsor interactions
Represent the organization as physician and subject matter expert during client meetings, scientific presentations, conferences, proposal discussions, and bid defense activities
Provide medical and scientific expertise during client feasibility assessments, including study design, patient populations, enrollment strategies, and site selection
Serve as Medical Monitor for assigned studies and provide medical oversight of patient safety, scientific rigor, and operational excellence
Review and interpret laboratory data, adverse events, medical coding dictionaries, and study data outputs
Review and provide expert input into medical monitoring plans, study protocols, statistical analysis plans, case report forms, training materials, investigator brochures, clinical study reports, and other study documents
Conduct independent medical analyses of emerging study data and communicate findings, risks, and recommendations
Collaborate with Safety/Pharmacovigilance teams on safety documentation, safety signal evaluation, and risk management
Contribute medical expertise to safety review meetings, data monitoring activities, and governance committees
Lead complex global clinical programs and guide regional medical leaders and project teams
Participate in investigator meetings and scientific advisory discussions
Mentor, coach, and develop Medical Directors, Associate Medical Directors, and other colleagues
Identify opportunities to improve processes, efficiencies, quality, client experience, scientific excellence, operational effectiveness, and innovation

Requirements

What you’ll need

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
At least 10 years combined experience in academic and/or industry clinical research in drug development
Experience as a Medical Monitor on clinical oncology and/or rare clinical trials is required
Clinical practice experience of a minimum of 3-5 years preferred
Board certification in hematology and/or oncology preferred
Effective written and verbal communication skills
Salesmanship and presentation skills
Proficiency and sensitivity to work in a global company with reports from varied cultures and backgrounds
Candidates must be legally authorized to work in the country of employment without employer sponsorship

Benefits

Comp & perks

Discretionary annual bonus
Health insurance
Retirement savings benefits
Life insurance
Disability benefits
Parental leave
Paid time off for sick leave and vacation