US Compliance Business Partner (Research &Development & Pain),Associate Director(Hybrid)
Vertex is a transformative biotechnology company that creates new possibilities in medicine to transform diseases and improve people’s lives. The company currently has five drugs on the market that treat the underlying cause of cystic fibrosis, one drug on the market that is a cell and gene therapy treatment for sickle-cell disease and transfusion-dependent t β-thalassemia, and one drug on the market for the treatment of acute pain. It has also developed a deep pipeline, investing billions of dollars into R&D over the past two decades.
Vertex is seekingan experienced Legal and Compliance professional to join its Office of Business Integrity & Ethics (OBIE) as theCompliance (OBIE) Business Partner for Global Research & Clinical Development. This individual would also be responsible for helping to support the US Pain Business Unit. OBIE is responsible for the development, implementation, oversight, and continuous improvement of Vertex’s Compliance Program. This includes defining standards via policies and procedures, creating, and implementing training and communications, conducting auditing and monitoring and other assurance activities, facilitating internal reporting, discretely and professionally conducting compliance-related investigations, and keeping the CEO, the Executive Committee, and the Board of Directors informed on compliance matters. OBIE serves as the go-to experts for Vertex employees and external stakeholders on issues relating to Vertex’s Compliance Program and Code of Conduct globally.
The person in this role will provide clear and actionable analysis, guidance and counselto Vertex’s Global Research & Clinical Development colleagues as well as colleagues within the Pain Business Uniton a broad array of strategic and tactical projects. The ideal candidate will have prior experience providing advice and guidance to prescription drug companies on legal issues relating to scientific exchange, external funding, patient support programs, and interactions with healthcare professionals and patient organizations. This role supports and reports to the Executive Director, Senior OBIE Business Partner Global/North Americaand works closely with OBIE Global, North America, International, and Operations colleagues providing clear and actionable analysis, guidance, and advice on the Program. The Business Partner must have strong, demonstrated knowledge of laws,regulations, and codes applicable to the pharmaceutical industry, including the US and international anti-bribery/anti-corruptions laws such as the Anti-Kickback Statute, False Claims Act, and Foreign Corrupt Practices Act and experience providing advice and counsel to biotechnology/pharmaceutical companies on these issues. Additionally, the Business Partner will work collaboratively with colleagues in OBIE, Legal, and the business to drive a culture of ethics and integrity across Vertex’s global organization.
you thrive in a dynamic, fast-paced, hands-on, and team-oriented environment where you can have a big impact on patients in need, their communities, and our organization, we’d love to speak with you!
Advise Global and North America business colleagues in Research & Clinical Developmentand the US Pain Business Unit on various initiatives in a way that advances the company’s 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 and advice on projects and initiativesto drive fact- and risk-based decision making.
Collaborate with the OBIE Training and Communications team on substantive trainings and regular communications on Compliance policies, procedures, and areas of risk.
Maintain a high level of knowledge of current and emerging laws, regulations, codes, and recent enforcement actions across the US and inform and educate business colleagues with tailored communications.
Help to establish standards and implement procedures to ensure the Compliance Program is effective and efficient.
Develop and maintain strong relationships and collaborate frequently with Legal, Human Resources, Internal Audit, and colleagues in other functional areas both in and outside of the US.
Support continuous improvement of the Global Compliance Program.
Qualifications, Professional Skills, and Preferred Experience
5-7 years post-JD experienceproviding legal counsel in the biotechnology/pharmaceutical industry, including both in-house at a global biotechnology or pharmaceutical company (strongly preferred) or a combination of law firm and in-house experience.
Outstanding ability to effectively communicate sound advice to lawyers and non-lawyers alike, coupled with a strong understanding of business needs.
Expert knowledge of statutes, regulations, and guidance documents applicable to commercial, developmentand medical affairs activities, including research and interpretation of 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 Codeand extensive experience providing legal counsel on these topics.
Demonstrated commitment to Compliance, ethics, and accountability.