Backed by Canaan Partners.
About the role
Tyra Biosciences, Inc. is seeking a highly motivated Senior Director of Regulatory Affairs, Oncology to make impactful contributions to rare disease drug discovery projects targeting disease areas with high unmet medical need. The successful candidate will be highly organized, self-motivated, and thrive in a dynamic, cross functional start-up environment. Found on 1752vc Careers, the job board for startup and VC roles.
What they're looking for
- Bachelor’s degree in a scientific discipline, advanced degree (MS, PhD, PharmD, or MD) strongly preferred
- 10+ years of progressive experience in global regulatory strategy within the biotechnology or pharmaceutical industry
- Mandatory experience leading late‑stage development and global registration for oncology products
- Demonstrated success with major global marketing applications (e.g., NDA/BLA/MAA) and health authority interactions
- Strong knowledge of global regulatory requirements and pathways for oncology drug development
- Proven ability to operate with urgency and make sound regulatory decisions in a fast‑paced environment
More about this role
Tyra Biosciences, Inc. is seeking a highly motivated Senior Director of Regulatory Affairs, Oncology to make impactful contributions to rare disease drug discovery projects targeting disease areas with high unmet medical need. The successful candidate will be highly organized, self-motivated, and thrive in a dynamic, cross functional start-up environment.
The Senior Director, Regulatory Affairs, Oncology will provide strategic regulatory leadership for a late‑stage oncology program in a rapidly growing biotechnology company. Reporting to the Vice President, Regulatory Strategy and Operations, this role is accountable for developing and executing global regulatory strategies that enable timely registration, approval, and lifecycle management of oncology products across major global markets.
This position requires a highly driven regulatory leader with deep global late‑stage and registration experience, proven oncology expertise, and the ability to lead with urgency in a fast‑moving environment.
Develop and execute comprehensive global regulatory strategies for a late‑stage oncology program, aligned with overall development, registration, and commercialization objectives.
Lead...
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