Clinical Development Medical Director (Hematology)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Location: Hybrid role based in New York City, United States, requiring residence within commuting distance and on-site work an average of 2.5 days per week. Candidates must have permanent authorization to work in the United States. U.S. visa sponsorship is not available.
Salary: $239,900–$399,800 annual base salary, plus a 25% bonus target and eligibility for a share-based long-term incentive program.
Company
is a global pharmaceutical company developing medicines and vaccines across multiple therapeutic areas.
What you will do
- Provide clinical development leadership across two to three hematology study teams.
- Oversee medical monitoring, eligibility assessment, clinical data review, and safety monitoring.
- Lead peer-to-peer discussions with investigators and address clinical issues with study teams, ethics committees, steering committees, and regulatory authorities.
- Develop and maintain clinical trial and regulatory documents with clinical scientists and cross-functional partners.
- Interpret clinical data, identify key findings, and communicate implications to internal and external stakeholders.
- Advise current and future clinical development plans using current medical literature, guidelines, and clinical expertise.
Requirements
- Clinical development experience.
- Medical degree such as MD, DO, MBBS, or MBChB from a recognized medical school or university.
- At least four years of experience after obtaining a medical degree.
- Medical license allowing independent prescription of medicines for at least two years after internship, house officer, or foundation training.
- Permanent U.S. work authorization is required; TN, O-1, H-1B, and other U.S. visa sponsorship is unavailable.
Nice to have
- Late-stage clinical development experience.
- Hematology experience.
- Board certification or eligibility in oncology or an equivalent qualification.
Culture & Benefits
- Cross-functional collaboration with regulatory affairs, pharmacovigilance, biostatistics, medical affairs, oncology teams, and external stakeholders.
- Opportunities to influence peers, coach colleagues, and guide work toward meaningful clinical and business outcomes.
- Comprehensive benefits including a 401(k) with company matching and an additional retirement savings contribution.
- Paid vacation, holidays, personal days, caregiver and parental leave, and medical leave.
- Medical, prescription drug, dental, and vision coverage.
- Travel to conferences and team meetings approximately four times per year; relocation assistance may be available based on eligibility and business needs.
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