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BeOne Medicines

Field Medical Director – Solid Tumor, Breast and Lung

BeOne Medicines

Field Medical Director coordinating research collaborations and strategies for solid tumor pipeline development. Working with healthcare providers and internal stakeholders within BeOne Medicines.

Posted 7/28/2026full-timeRemote • Connecticut, Maine, Massachusetts, New Hampshire, New Jersey, New York, Rhode Island, Vermont • 🇺🇸 United StatesLead💰 $215,400 - $275,400 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical oncology with a focus on solid tumors, while effectively managing relationships with healthcare providers and coordinating clinical trial activities. Strong communication and organizational skills are essential for successful collaboration in a global environment.

Highest-signal resume keywords
Clinical Oncology ExperienceClinical Trial CoordinationHealthcare Provider RelationshipsCommunication SkillsCross-Functional Collaboration

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 ExperienceOncology ExpertiseInvestigator VettingRegional Strategy DevelopmentFormulary Decision Support
Soft Skills
Interpersonal SkillsOrganizational SkillsFlexibilityCollaboration Skills
Certifications & Qualifications
MDPharmDPhDDONPPA
Industry Keywords
Solid TumorsClinical Pipeline DevelopmentOpinion LeadersResearch CollaboratorsWork-Related Travel

About the role

Key responsibilities & impact
  • Support BeOne Medicines pre-clinical and clinical pipeline development by coordinating external collaborations with healthcare providers
  • Develop regional strategies for relationships with opinion leaders and research collaborators
  • Provide balanced, accurate information to regional formulary decision makers when requested
  • Identify and vet investigators for company-sponsored clinical trials and serve as a liaison for investigator-sponsored research

Requirements

What you’ll need
  • MD, PharmD., PhD, or DO with a minimum of 5 years’ clinical experience or NP, PA, Master’s Degree with a minimum of 6 years’ clinical experience
  • Clinical oncology experience in solid tumors
  • Relationships with relevant HCPs in region
  • High level of communication (written and verbal), interpersonal, organizational, and cross functional collaboration skills
  • Flexibility to work with colleagues in a global setting
  • Able to engage in work-related travel approximately 60-70%

Benefits

Comp & perks
  • Medical
  • Dental
  • Vision
  • 401(k)
  • FSA/HSA
  • Life Insurance
  • Paid Time Off
  • Wellness