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BeOne Medicines

Senior Field Medical Director – Florida/PR

BeOne Medicines

Senior Field Medical Director supporting oncology pipeline development at BeOne. Coordinating with internal and external teams for robust scientific collaboration.

Posted 6/5/2026full-timeRemote • Florida • 🇺🇸 United StatesSenior💰 $258,400 - $328,400 per yearWebsite

About the role

Key responsibilities & impact
  • Support BeOne Pre-Clinical and Clinical pipeline development by coordinating external collaborations, research endeavors with health care providers and external academicians while ensuring internal partnership across the organization.
  • Report to the Senior Regional Director, Hematology, within Medical Affairs.
  • Develop regional strategies to support enduring and compliant relationships with Opinion Leaders, Research Collaborators & Key Organizations in support of BeOne pipeline development (Solid Tumor or Hematology).
  • Provide pre-launch and post-launch Medical Affairs support for hematology pipeline development.
  • Work closely with internal colleagues in medical affairs, clinical development, program leadership, clinical operations, legal, compliance, new product planning, safety/pharmacovigilance, molecular diagnostics, marketing, sales and translational research.
  • Play a key role in the establishment of BeOne as a valued collaborator and best-in-class biopharmaceutical company.
  • Work with Cross-functional teams to develop robust territory plans that impact and inform HCPs leading to improved patient outcomes.
  • Establish and maintain scientifically credible peer-to-peer scientific relationships with national & regional opinion leaders in addition to other healthcare providers.
  • Facilitate & monitor strategic partnerships with scientific/clinical experts and serve as an enterprise-level point of contact with organizations including but not limited to - Guideline development, Cooperative groups, Other (National Cancer institutions).
  • Serve as an internal resource of clinical and scientific information from medical interactions.
  • Provide impactful feedback/information to internal stakeholders on emerging clinical and scientific trends.
  • Nominate sites to Clinical Operations to participate in clinical research.
  • Contribute to or perform therapeutic area/indication research and competitor analysis.
  • Assist in the development and execution of clinically relevant regional medical meetings (e.g., advisory boards, consultant, and investigator meetings), as requested.
  • Identification and verification of investigators and sites for company-sponsored clinical trials.
  • Serve as a liaison for the submission and review of Investigator Sponsored Research proposals.
  • Support major and regional congresses engaging thought leaders.
  • Build strong relationships with internal experts.
  • Identify continuous process improvement opportunities.
  • Develop, track, execute and report on goals and objectives.
  • Support Medical Affairs budget planning and management.
  • Be accountable for compliant business practices.

Requirements

What you’ll need
  • MD, PharmD., PhD, or DO, within a clinical and/or scientific profession with 6 + years’ clinical experience and/or success within other biotech/pharmaceutical companies OR a NP, PA, Master’s Degree within a clinical and/or scientific profession with 8 + years’ clinical experience and/or success within other biotech/pharmaceutical companies.
  • Clinical oncology experience in hematology/oncology.
  • 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%.
  • Impactful verbal and written communication skills.
  • Ability to effectively collaborate in a dynamic environment.
  • Strong comprehension of disease states, and knowledge of differential algorithms for treatment decisions and experience in disease states of interest to BeOne.
  • An expert understanding of the health care delivery system, including the managed care arena and its impact on patient care, regional medical care and the pharmaceutical industry.
  • Ability to identify the unmet medical, educational, and research needs at a local & regional level in the medical community.
  • Ability to interpret key scientific data and translate the findings to meet educational and research needs in order to affect corporate research strategic activities/decisions.
  • Understanding of the design and execution of research studies and strategic implications.
  • Exhibits high degree of emotional intelligence and appreciation of diversity and multiculturalism.
  • Designs and/or leads training initiatives and best practices.
  • Proven ability to drive results at a high level of quality as a strategic and creative thinker.
  • Demonstrates ability to deal with ambiguity and thrive in an ever-changing environment.
  • Strong project management skills with demonstrated ability to manage projects and/or colleagues in successful implementation of business-critical projects.
  • Strong time management & organizational skills.

Benefits

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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
clinical oncologyhematologydisease state comprehensiondifferential algorithmsresearch study designclinical trial managementinvestigator sponsored researchclinical experiencebiotech experiencepharmaceutical experience
Soft Skills
communication skillsinterpersonal skillsorganizational skillscross functional collaborationflexibilityemotional intelligenceproject managementtime managementstrategic thinkingadaptability
Certifications
MDPharmDPhDDONPPAMaster’s Degree