Medical Director, Hematology

🕒 January 9

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BeOne Medicines

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 2010

BeOne Medicines is a global oncology company domiciled in Switzerland that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a portfolio spanning hematology and solid tumors, BeOne is expediting development of its diverse pipeline of novel therapeutics through its internal capabilities and collaborations. With a growing global team of more than 11,000 colleagues spanning six continents, the Company is committed to radically improving access to medicines for far more patients who need them.

📋 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.

🎯 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