Cancer has no borders. Neither do we.
Medical Director, Hematology
Location
United States
Posted
169 days ago
Salary
$249.8K - $309.8K / year
Seniority
Lead
Job Description
Medical Director, Hematology
BeOne Medicines
• 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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