2 часа назад
Medical Director, Pulmonary (Immunology)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Medical Director, Pulmonary (Immunology): Developing and executing integrated U.S. medical strategies for pulmonary products with an accent on clinical evidence generation, medical engagement, and cross-functional alignment. Focus on designing and overseeing Phase IIIB-IV studies, reviewing scientific and promotional materials, managing safety data, and guiding advisory-board and stakeholder relationships.
Location: Hybrid role based in Cambridge, Massachusetts or Morristown, New Jersey, United States; travel up to 35% required.
Company
is an R&D-driven, AI-powered biopharmaceutical company developing medicines for immune challenges, rare diseases, cancers, and neurological conditions.
What you will do
- Develop and execute integrated U.S. medical strategies and annual budgets for pulmonary products.
- Lead medical education, communications, publications, health outcomes, safety, clinical research, and investigator-sponsored trial activities.
- Partner with Clinical, Commercial, Regulatory, Market Access, Health Economics, Drug Safety, global teams, and field medical teams.
- Generate and communicate scientific insights, provide medical expertise, and manage relationships with physicians, researchers, payers, and other stakeholders.
- Review and approve medical, scientific, promotional, regulatory, safety, training, and grant materials for compliance with applicable standards and regulations.
- Oversee Phase IIIB-IV studies, registries, safety activities, research collaborations, advisory boards, and timely publication of generated data.
Requirements
- Advanced degree in life sciences or pharmaceutical sciences, such as PhD, PharmD, PA, NP, or MD with relevant experience.
- At least 5 years of relevant Medical Affairs experience and a strong record of developing and executing U.S. medical strategies.
- Clinical or Medical Affairs experience in Pulmonary and/or Immunology is strongly preferred.
- Industry experience in Medical Affairs or Clinical Development, including launch and life-cycle management activities.
- Strong understanding of clinical-trial design and execution, pharmacovigilance, healthcare systems, regulatory requirements, and payer environments.
- Excellent scientific communication, leadership, stakeholder-management, analytical, prioritization, and cross-functional collaboration skills.
Culture & Benefits
- Work in a supportive, future-focused environment centered on improving patient outcomes.
- Opportunities for career growth through promotion or lateral international moves.
- Rewards package with employee benefits and healthcare coverage.
- Health, prevention, and wellness programs, plus at least 14 weeks of gender-neutral parental leave.
- Commitment to ethical standards, scientific integrity, teamwork, and a culturally diverse workforce.
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