The Executive Director or VP will lead global regulatory strategy for oncology programs from pre-IND through commercialization and lifecycle management. They will act as the primary liaison with health authorities and oversee the preparation and submission of critical regulatory documents. Candidates must have an undergraduate degree and at least 10 years of relevant experience in pharmaceutical or biotech regulatory affairs. Deep expertise in global regulatory strategy and proven experience leading interactions with the FDA and other health authorities are required.
Erasca provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
