BeOne Medicines

Senior Medical Director, Hematology

BeOne Medicines

full-time

Posted on:

Location Type: Remote

Location: United States

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Salary

💰 $299,800 - $369,800 per year

Job Level

About the role

  • Support BeOne Clinical and Medical Hematology assets by successful execution of clinical development programs and deliverables in partnership across the organization
  • Involved in clinical program strategy and help assure that activities are executed within expected scope, budget and timelines
  • Work closely with colleagues in clinical development, program leadership, biometrics, clinical operations, safety/ pharmacovigilance, regulatory, molecular diagnostics, and translational research
  • Facilitate generation of, author, update, and/or review key documents
  • Partner with clinical operations and other functional areas for the successful implementation and execution of clinical studies
  • Provide scientific expertise for selection of investigator and vendors
  • Train colleagues, CRO staff, and study site staff
  • Provide scientific and medical support throughout conduct of a clinical trial
  • Review, query, and analyze clinical trial data
  • Interpret, and present clinical trial data both internally and externally
  • Represent a clinical study or development program on one or more teams or sub teams
  • Create clinical study or program-related slide decks for internal and external use
  • Build and maintain opinion leader/investigator networks

Requirements

  • 6 plus years of experience within other biotech/pharmaceutical or relevant academic credentials companies
  • Advanced degree (MD or MD equivalent) with subspecialty training in hematology/oncology (preferred)
  • Previous participation in a clinical development program is essential, including involvement in all stages of clinical trials (i.e. from start up to study report)
  • Clinical oncology experience: candidates with exceptional experience in other therapeutic areas would be considered if they demonstrated clear potential to apply their existing skills to oncology
  • Expert understanding of global clinical study design and drug development process from discovery to registration and post-marketing
  • High level of communication (written and verbal), interpersonal, organizational, and cross functional collaboration skills
  • Knowledge of GCP and ICH Guidelines
  • Flexibility to work with colleagues in a global setting
  • Strategic leader with demonstrated success building, managing and developing individuals and teams is preferred
  • Experience with the development and support of related SOPs and policies is expected
  • Knowledge of industry standard Clinical Development IT solutions expected
Benefits
  • Medical
  • Dental
  • Vision
  • 401(k)
  • FSA/HSA
  • Life Insurance
  • Paid Time Off
  • Wellness
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical developmentclinical trial managementdata analysisclinical study designdrug development processGCPICH GuidelinesSOP developmentoncology expertisebiometrics
Soft Skills
communicationinterpersonal skillsorganizational skillscross functional collaborationstrategic leadershipteam managementtrainingflexibilitypresentation skillsscientific expertise
Certifications
MDMD equivalentsubspecialty training in hematology/oncology