
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
Tech Stack
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