3 дня назад
Associate Director, Healthcare Compliance
171 000 - 209 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Associate Director, Healthcare Compliance (Biopharmaceutical Compliance): Building and continuously improving Intellia’s Healthcare Compliance Program for the commercialization of a gene editing therapy for hereditary angioedema with an accent on risk-based monitoring, compliance assessments, and transparency reporting. Focus on leading monitoring plans, overseeing reportable transaction data, applying Compliance by Design principles, and managing complex cross-functional compliance initiatives.
Location: Onsite in Cambridge, Massachusetts, United States; travel of 15–20% required
Salary: $171,000–$209,000 USD per year, plus performance-based annual bonus and equity compensation
Company
develops curative genome-editing treatments for severe and life-threatening diseases, including a therapy for hereditary angioedema.
What you will do
- Build, implement, and continuously improve the Healthcare Compliance Program supporting commercialization of a gene-editing therapy.
- Develop and lead the annual risk-based monitoring plan based on ongoing risk assessments and emerging compliance needs.
- Oversee live and transaction monitoring, using emerging technologies such as AI to improve efficiency and accuracy.
- Partner with Legal, Commercial, Medical Affairs, and other functions on compliance assessments and auditable record-keeping.
- Serve as the subject matter expert on the Physician Payments Sunshine Act, aggregate spend reporting, and state transparency requirements.
- Lead compliance project initiatives, identify trends and gaps, and report improvement opportunities to senior leadership.
Requirements
- 6+ years of healthcare compliance or related experience in a commercial-stage biotech or pharmaceutical organization.
- Experience in the biopharmaceutical industry and knowledge of commercial activities, including sales and marketing, healthcare professional and patient interactions, and patient support services.
- General knowledge of pharmaceutical laws, regulations, and industry guidance related to commercialization.
- Bachelor’s degree required.
- Ability to independently lead projects from inception to completion with minimal supervision.
- Strong communication, organizational, relationship-building, conflict-management, and attention-to-detail skills.
Nice to have
- Experience launching products in a commercial-stage organization.
- Rare disease experience.
Culture & Benefits
- Work guided by the values One, Explore, Disrupt, and Deliver.
- Opportunity for visibility with senior leadership and continued professional development.
- Performance-based annual cash bonus.
- New-hire equity grant and eligibility for annual equity awards.
- Commitment to diversity, inclusion, and equal employment opportunity.
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