SVP Regulatory Affairs & Quality — Global Strategy & Compliance

Dennis Partners; United States; Hybrid; USD 350,000 - 450,000; Full time

Benefits offered by this job

Annual target bonus

Equity

Comprehensive benefits

Job summary

Dennis Partners is seeking a VP or SVP, Head of Regulatory Affairs and Quality to lead all regulatory strategies at their biopharmaceutical company. This critical position oversees the development and commercialization of therapies targeting debilitating diseases.

The successful candidate will provide leadership to the Regulatory and Quality Organization, ensuring compliance with regulations and leading teams in oncology and neuroscience programs. This is a hybrid position based in Connecticut.

Qualifications

• A minimum of 20 years of Regulatory Affairs experience in the biopharmaceutical industry.
• Extensive Regulatory experience with oncology programs.
• Strong ex-US/global regulatory experience required.

Responsibilities

• Oversee all regulatory strategies and lead communications with Health Authorities.
• Develop and implement global regulatory strategies for oncology and neuroscience programs.
• Provide leadership to the Regulatory and Quality Organization.

Skills

Regulatory Affairs

Oncology programs

CNS/neuroscience programs

Leadership

Communication

Education

Bachelors in a scientific discipline

Advanced degree (MS, MD PharmD, or PhD)

Job description

Dennis Partners is seeking a VP or SVP, Head of Regulatory Affairs and Quality to lead all regulatory strategies at their biopharmaceutical company. This critical position oversees the development and commercialization of therapies targeting debilitating diseases.

The successful candidate will provide leadership to the Regulatory and Quality Organization, ensuring compliance with regulations and leading teams in oncology and neuroscience programs. This is a hybrid position based in Connecticut.