3 дня назад
Scientific Director / Senior Medical Director, Medical Affairs Parkinsons Disease, US
182 000 - 346 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Scientific Director / Senior Medical Director, Medical Affairs Parkinsons Disease, US (Neuroscience): Leading medical affairs strategy and scientific activities for a Parkinson’s disease asset with an accent on evidence generation, scientific communications, and cross-functional development strategy. Focus on shaping clinical development plans and protocols, interpreting safety and efficacy data, and coordinating regulatory and medical activities across matrixed teams.
Location: Mettawa, Illinois, United States; hybrid schedule with office attendance Tuesday through Thursday
Salary: $182,000–$346,000 per year
Company
develops medicines and healthcare solutions across immunology, oncology, neuroscience, and aesthetics.
What you will do
- Set and drive medical affairs strategy for a key Parkinson’s disease asset within the Neuroscience portfolio.
- Lead data generation and dissemination strategies, Medical Affairs Plans, and Brand Plans.
- Coordinate scientific and medical activities with commercial, market access, HEOR, clinical operations, clinical development, and regulatory stakeholders.
- Engage scientific experts and support marketing materials, medical education programs, advisory activities, and symposia.
- Provide scientific and medical education to investigators, clinical monitors, and Global Project Team members.
- Ensure scientific programs meet budget, timeline, and compliance requirements; M.D. holders may oversee Medical Affairs-led studies and interpret safety and efficacy data.
Requirements
- Scientific Director: PhD or PharmD and 7–10 years of Medical Affairs experience across evidence generation, scientific communications, KOL engagement, and cross-functional strategy.
- Senior Medical Director: M.D., D.O., or equivalent degree and at least 2 years of clinical trial or pharmaceutical medical affairs experience; 3+ years preferred.
- Knowledge of real-world evidence, investigator-initiated and company-sponsored studies, registries, medical insights, promotional review, and brand strategy.
- Knowledge of clinical trial methodology, data analysis and interpretation, regulatory requirements, development strategy, and protocol design.
- Proven leadership in a cross-functional global team environment.
- Excellent written and spoken English communication skills required.
Culture & Benefits
- Hybrid work at the Mettawa headquarters with regular in-office collaboration.
- Paid vacation, holidays, and sick leave.
- Medical, dental, and vision insurance for eligible employees.
- 401(k) benefits for eligible employees.
- Eligibility to participate in long-term incentive programs.
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