обновлено 7 дней назад
Clinical Development Senior Medical Director, Breast Oncology
274 500 - 457 500$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Clinical Development Senior Medical Director, Breast Oncology (Clinical Trials/Oncology): Leading clinical development activities for the atirmociclib program, including medical monitoring, study-team leadership, regulatory documentation, and clinical data interpretation with an accent on scientific, ethical, and regulatory rigor. Focus on guiding multiple study teams, shaping late-phase development strategies, leading marketing authorization subteams, and collaborating with investigators, health authorities, and cross-functional stakeholders.
Location: Hybrid role based in New York City, United States, requiring on-site work an average of 2.5 days per week and residence within commuting distance. Candidates must have permanent U.S. work authorization; visa sponsorship is not available.
Salary: $274,500–$457,500 annually, 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 multiple study teams and development subteams.
- Conduct medical monitoring, including eligibility assessments, clinical data review, and safety monitoring.
- Lead peer-to-peer interactions with investigators and coordinate clinical issues with study teams, ethics committees, steering committees, and regulatory authorities.
- Lead and contribute to clinical trial and regulatory documentation with Clinical Scientists and cross-functional partners.
- Collaborate with Global Development Teams to shape development strategies and interpret clinical data.
- Represent in external scientific engagements and lead subteams supporting Marketing Authorization Applications.
Requirements
- Primary medical degree such as MD, DO, MBBS, or MBChB from a recognized medical school or university.
- At least 4 years of biopharmaceutical industry experience in clinical research and development.
- At least 2 years of independent prescribing licensure after completing the intern, house officer, or foundation period.
- Breast oncology experience of at least 2 years.
- Permanent authorization to work in the United States by any employer; U.S. work visa sponsorship is not available now or in the future.
- Ability to live within commuting distance of the New York City worksite and work on-site an average of 2.5 days per week.
Nice to have
- Board certification or eligibility in oncology, or equivalent qualification.
- Late-phase clinical development experience.
- Demonstrated leadership, collaboration, influencing, coaching, and team-guidance capabilities.
Culture & Benefits
- Hybrid work arrangement with occasional travel to scientific conferences and meetings.
- Participation in ’s Global Performance Plan with a 25% bonus target.
- Eligibility for a share-based long-term incentive program.
- 401(k) plan with matching contributions 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.
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