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5 дней назад

Associate Director, Healthcare Compliance (Biotech)

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 (Biotech): Building and continuously improving a healthcare compliance program for the commercialization of a gene editing therapy, with an accent on risk-based monitoring, compliance assessments, and transparency reporting. Focus on developing monitoring plans, overseeing transaction reporting under the Physician Payments Sunshine Act, using AI-enabled monitoring solutions, and leading cross-functional compliance initiatives.

Location: Cambridge, Massachusetts, United States; travel of 15–20% required.

Base salary: $171,000–$209,000 per year, plus performance-based annual cash bonus and equity compensation.

Company

hirify.global is a biotechnology company developing CRISPR/Cas9-based genome editing medicines and engineered cell therapies for genetic diseases, cancer, and autoimmune diseases.

What you will do

  • Build, implement, and continuously improve the healthcare compliance program supporting commercialization of a gene editing therapy for hereditary angioedema.
  • Develop and lead an annual risk-based monitoring plan based on compliance assessments and emerging risks.
  • Conduct live and transaction monitoring, using emerging technologies and AI solutions to improve efficiency and accuracy.
  • Identify compliance trends and gaps, report findings to senior leadership, and recommend improvements.
  • Oversee the collection, compilation, and reporting of transactions under the Physician Payments Sunshine Act and state transparency requirements.
  • Lead compliance projects and collaborate with Commercial, Medical Affairs, Legal, and other cross-functional teams.

Requirements

  • B.A. or B.S. degree required.
  • 6+ years of healthcare compliance or related experience in a commercial-stage biotechnology or pharmaceutical organization.
  • Knowledge of pharmaceutical laws, regulations, and industry guidance related to commercialization of biopharmaceutical products.
  • Experience with commercial activities including sales and marketing, healthcare professional and patient engagement, and patient support services.
  • Ability to independently lead projects, deliver presentations and training, manage conflict, and build relationships in a cross-functional environment.
  • Strong integrity, judgment, communication, organization, attention to detail, and collaboration skills required.

Nice to have

  • Experience with product launches or rare diseases.

Culture & Benefits

  • Mission focused on developing curative genome editing treatments for severe and life-threatening diseases.
  • Work aligned with the values One, Explore, Disrupt, and Deliver.
  • Visibility to senior leadership and opportunities for continued development.
  • Performance-based annual cash bonus and new hire equity grant.
  • Eligibility for annual equity awards and company benefits.

Hiring process

  • Applications are accepted on a rolling basis until the position is filled.

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