Vice President, Regulatory Affairs
Nuvalent, Inc.
full-time
Posted on:
Location Type: Remote
Location: Remote • Massachusetts • 🇺🇸 United States
Visit company websiteSalary
💰 $315,000 - $340,000 per year
Job Level
Lead
About the role
- Reporting to the Chief Development Officer, the Vice President of Regulatory Affairs / Alliance Management will serve as a senior regulatory leader.
- Responsible for developing and executing global regulatory strategies across the company’s pipeline.
- Oversee regulatory submissions and interactions with global health authorities.
- Ensure programs progress efficiently and compliantly from early development through approval and commercialization.
Requirements
- 15+ years of regulatory affairs experience in biotech/pharma, with significant leadership in CDx or IVD development.
- Proven track record of successful regulatory submissions and approvals for CDx products, ideally in oncology.
- Expertise with major global submissions and late stage or approved programs
- Demonstrated success leading regulatory strategy for oncology therapeutics.
- Strong leadership, strategic thinking, and executive communication skills.
Benefits
- medical, dental, and vision insurance
- 401(k) retirement savings plan
- generous paid time off (including a summer and winter company shutdown)
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
regulatory affairsregulatory submissionsregulatory strategyCDx developmentIVD developmentoncology therapeuticsglobal health authoritiespipeline managementcomplianceexecutive communication
Soft skills
leadershipstrategic thinking