A company is looking for a US Lead - Oncology, Global Regulatory Policy & Innovation.
Key Responsibilities
Anticipate and influence US regulatory policy affecting drug development
Develop relationships with US regulators and key stakeholders in the regulatory landscape
Provide strategic guidance to product teams on regulatory changes and advocacy initiatives
Required Qualifications
PhD, PharmD, MD, or equivalent strongly preferred
Minimum of 15 years of experience in the pharmaceutical industry or regulatory policy
Strong knowledge of US drug regulations and guidance
Experience managing external partnerships with advocacy organizations and contractors
Proven success in stakeholder engagement across organizational levels
Regulatory Lead • Port Saint Lucie, Florida, United States