Senior Global Regulatory Director, Oncology (Remote)

Tyra Biosciences, Inc.; United States; Remote; USD 275,000 - 303,000; Full time

Benefits offered by this job

Competitive base salary

Annual bonus opportunities

Equity grants

Comprehensive health benefits

401(k) plan with match

Paid time off and holidays

Job summary

Tyra Biosciences, Inc. is seeking a Senior Director of Regulatory Affairs, UTUC to provide strategic regulatory leadership for a late‑stage oncology program.

You will develop global regulatory strategies, lead submissions, and guide interactions with health authorities across major markets. In a fast-moving startup environment, you will mentor teams, partner with cross-functional groups, and drive expedited pathways where applicable, while ensuring timely registration and lifecycle management of

Qualifications

• Bachelor’s degree in a scientific discipline; advanced degree preferred.
• 10+ years in global regulatory strategy.
• Experience leading late‑stage development and global registration for oncology.
• Proven success with major global marketing applications and health authority interactions.
• Ability to operate with urgency in a fast-paced environment.
• Strong written and verbal communication skills.

Responsibilities

• Develop and execute global regulatory strategies for a late‑stage oncology program.
• Lead global health authority interactions (FDA, EMA, and others).
• Guide regulatory input into submissions, labeling, and lifecycle management.
• Mentor and lead cross‑functional teams; drive expedited pathways where applicable.

Skills

Regulatory leadership

Global strategy

Oncology experience

FDA/EMA interactions

Cross-functional leadership

Education

Bachelor’s degree in a scientific discipline

Advanced degree (MS/PhD/PharmD/MD) preferred

Job description

Tyra Biosciences, Inc. is seeking a Senior Director of Regulatory Affairs, UTUC to provide strategic regulatory leadership for a late‑stage oncology program.

You will develop global regulatory strategies, lead submissions, and guide interactions with health authorities across major markets. In a fast-moving startup environment, you will mentor teams, partner with cross-functional groups, and drive expedited pathways where applicable, while ensuring timely registration and lifecycle management of