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3 дня назад

Associate Director, Healthcare Compliance

171 000 - 209 000$
Формат работы
onsite
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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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

hirify.global 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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