BeOne Medicines logo
BeOne Medicines

Cancer has no borders. Neither do we.

Medical Director, Hematology

Medical DirectorMedical DirectorFull TimeRemoteLeadTeam 10,001+Since 2010H1B No SponsorCompany SiteLinkedIn

Location

United States

Posted

68 days ago

Salary

$249.8K - $309.8K / year

Seniority

Lead

Professional CertificateEnglishGoogle Cloud Platform

Job Description

• Support BeOne clinical assets and pipeline by successful execution of clinical development programs and deliverables in partnership across the organization, with external vendors, and with external academicians and collaboration partners. • Assess and execute clinical programs and help assure that activities are executed within expected scope, budget and timelines. • Establish and grow Clinical Research functions to assure best-in-class global capabilities and execution. • Work closely with colleagues in clinical development, program management, biometrics, clinical operations, safety/pharmacovigilance, regulatory, molecular diagnostics, and translational research and other functions. • Facilitate generation of key documents, including protocols, informed consent documents, Investigator Brochures, clinical study reports, and more. • Partner with clinical operations and other functional areas for successful implementation and execution of clinical studies. • Provide scientific expertise for selection of investigator and vendors. • Train BeOne colleagues, study site staff on the therapeutic area, molecule, and/or clinical protocol. • Review, query, and analyze clinical trial data; interpret, and present clinical trial data both internally and externally.

Job Requirements

  • MD (or equivalent medical degree); board certification or eligibility in relevant therapeutic area (e.g., oncology, hematology)
  • Clinical training with experience in drug development or clinical research, ideally across Phases I–III
  • Strong understanding of clinical trial design, GCP and regulatory environment for submissions (IND, CTA, NDA, BLA)
  • Demonstrated safety oversight skills, familiarity with DSURs, PSURs, and safety committees
  • Excellent communication skills, capable of engaging internal teams, external partners, and regulators.
  • Proven track record in therapeutic area development (hematology or oncology)
  • Experience or familiar with translational medicine, PK/PD data integration, or biomarker strategies.
  • Prior involvement with Life Cycle Management and commercial interfacing
  • Global clinical trial experience across multiple geographies

Benefits

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

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