via Ladders
$150K - 250K a year
Lead development of non-clinical and clinical regulatory strategies and manage global regulatory submissions for oncology products.
Advanced scientific degree and at least 15 years biopharmaceutical experience including 10 years in oncology regulatory affairs.
Strategic Regulatory Leader in Oncology The company is seeking a strategic thought partner to lead the development of non-clinical and clinical regulatory strategies. • Manage IND and NDA submissions globally. • Support all aspects of global commercial product regulatory affairs. Key qualifications include: • Advanced degree in a relevant scientific discipline. • Minimum 15 years' biopharmaceutical experience, including 10 years in regulatory affairs in oncology.
This job posting was last updated on 11/24/2025