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Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Director Compliance Business Partner

Regulatory Compliance & EthicsConfirmed live in the last 24 hours
Full-timeBoston, MA, USA

About the Job

Requirements

  • 8–10 years of post-JD experience providing legal counsel in the biotechnology or pharmaceutical industry, including in-house experience at a global biotechnology or pharmaceutical company or a combination of law firm and in-house experience.
  • Strong demonstrated knowledge of laws, regulations, and codes applicable to the pharmaceutical industry, including United States and international anti-bribery and anti-corruption laws such as the Anti-Kickback Statute, False Claims Act, and Foreign Corrupt Practices Act, and experience advising biotechnology or pharmaceutical companies on these issues.
  • Ability to communicate sound advice effectively to lawyers and non-lawyers, with a strong understanding of business needs.
  • Expert knowledge of statutes, regulations, and guidance applicable to commercial, development, and medical affairs activities, including the Food, Drug, and Cosmetic Act; FDA regulations and guidance; federal and state anti-kickback statutes; OIG guidance documents and advisory opinions; the False Claims Act; and the PhRMA Code, with extensive experience providing legal counsel on these topics.
  • Commitment to compliance, ethics, and accountability.
  • Ability to work in a fast-paced, dynamic environment.
  • Ability to travel as needed.
  • Proficiency in Microsoft Office, especially PowerPoint, Word, and Excel.
  • A law degree and legal experience are required.
  • Ability to communicate, present, and train effectively with all levels of management and employees.
  • Experience taking ownership of issues and providing timely, practical, and actionable guidance.
  • Strong oral and written communication and influencing skills, and ability to collaborate cross-functionally proactively and pragmatically.
  • Strong analytical, organizational, and problem-solving skills.
  • Project management skills and ability to manage multiple priorities simultaneously.
  • Self-starter with leadership skills and ability to meet goals; sound judgment in balancing risks in ambiguous and complex situations and escalating matters appropriately.
  • Ability to identify areas for improvement in controls, systems, and processes and implement effective solutions.
  • Ability to work with large amounts of data, analyze information, and maintain a broad perspective.
  • Confidence and professionalism in handling difficult conversations and discretion on sensitive matters.

Responsibilities

  • Advise global and United States business colleagues on initiatives in a way that advances company strategy while addressing legal and compliance risks and protecting the company’s integrity and reputation.
  • Serve as the Compliance representative on leadership and cross-functional teams, providing strategic and tactical guidance on projects and initiatives to support fact- and risk-based decision-making.
  • Collaborate with the OBIE Training and Communications team on substantive training and regular communications about Compliance policies, procedures, and risk areas.
  • Maintain knowledge of current and emerging laws, regulations, codes, and recent United States enforcement actions, and inform and educate business colleagues through tailored communications.
  • Help establish standards and implement procedures to ensure the Compliance Program is effective and efficient.
  • Develop strong relationships and collaborate frequently with Legal, Human Resources, Internal Audit, and colleagues in other functional areas in and outside the United States.
  • Support continuous improvement of the Global Compliance Program.

Desired Qualifications

  • In-house experience at a global biotechnology or pharmaceutical company is strongly preferred.

About the Company

Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Vertex Pharmaceuticals develops medicines for serious diseases, with a focus on cystic fibrosis. It conducts extensive research and partners with other biotech firms to discover and develop new therapies, including ex vivo engineered cell treatments. Its products, such as ivacaftor, treat cystic fibrosis and other therapies undergo clinical testing to expand the pipeline. Revenue comes from selling approved drugs and from licensing and collaboration agreements. The company distinguishes itself through deep R&D investment, strategic partnerships, and a global reach aimed at addressing unmet medical needs. The overall goal is to bring effective new drugs to patients worldwide and improve outcomes and quality of life.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Boston, MA
Founded
1989

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