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Precision For Medicine

Senior Medical Director – Oncology

Precision For Medicine

. Provide strategic medical, scientific, and operational leadership across clinical development programs .

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

Core Competencies

Role fit
Core Competencies

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Demonstrates strategic leadership in clinical development, providing medical oversight and expertise in oncology and hematology. Capable of guiding cross-functional teams and enhancing operational excellence through effective communication and mentorship.

Highest-signal resume keywords
Medical Monitor ExperienceClinical Research ExpertiseOncology and Hematology Board CertificationStrategic Leadership in Clinical DevelopmentEffective Communication Skills

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Trial DesignData MonitoringMedical OversightStatistical Analysis PlansAdverse Event ReviewLaboratory Data InterpretationMedical CodingPatient Safety ManagementIndependent Medical AnalysisProcess Improvement
Soft Skills
Effective Written CommunicationPresentation SkillsSalesmanshipMentoring and CoachingCross-Cultural Sensitivity
Certifications & Qualifications
MDDOMBBSBoard Certification in HematologyBoard Certification in Oncology
Industry Keywords
Clinical Development ProgramsDrug DevelopmentFeasibility AssessmentsGlobal Clinical ProgramsSafety/PharmacovigilanceScientific PresentationsBid Defense MeetingsInvestigator MeetingsClinical Study ReportsGovernance Committees

About the role

Key responsibilities & impact
  • Provide strategic medical, scientific, and operational leadership across clinical development programs
  • Serve as a trusted advisor to sponsors, investigators, and cross-functional teams
  • Represent the organization as medical and scientific authority in client interactions, proposal development, bid defense meetings, scientific presentations, and industry conferences
  • Support 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
  • Provide expert input into medical monitoring plans, 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, signal evaluation, and risk management
  • Contribute 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, efficiency, quality, client experience, scientific excellence, 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 working in a global company with reports from varied cultures and backgrounds
  • 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