VP Clinical Development & Global Program Lead, Lung Cancer
Erasca · San Diego, CA; South San Francisco, CA; remote
Posted 27 days ago · $390,000 to $435,000
or apply directly on Erasca's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 27 days Erasca's roles stay open a median of 43 days
- Reposted
- No
- Salary listed
- Yes 100% of Erasca's roles list one
- Ghost-job risk at Erasca
- high 5 stale, 0 reposted of 10 open
- Hiring momentum
- 13 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Erasca's own greenhouse board since 2026-08-03. Full hiring picture for Erasca.
About this role
The VP Clinical Development & Global Program Lead for Lung Cancer at Erasca will oversee the lung cancer development program, collaborating closely with the Chief Medical Officer. This role involves leading clinical development strategies, designing clinical trials, ensuring regulatory compliance, and mentoring a team of medical directors and clinical scientists. The VP will also engage with key opinion leaders and contribute to scientific publications and presentations.
- benefits
- 5/5
- freshness
- 4/5
- career value
- 5/5
- role clarity
- 5/5
- pay transparency
- 5/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Erasca as an employer.
What you need
- M.D. degree or equivalent with subspecialty fellowship training and board certification or eligibility in Oncology or Oncology/Hematology
- 8-10+ years of oncology clinical trial and drug development experience in the pharmaceutical or biotechnology industry
- Experience as the clinical lead on late-stage clinical programs in lung cancer
- Experience leading or closely involved in clinical aspects of regulatory filings and direct interaction with health authorities
- Extensive knowledge of clinical trial methodology and regulatory compliance requirements
- Demonstrated ability to collaborate successfully with multiple functions in a matrixed team environment
Nice to have
- Additional training and clinical practice experience in thoracic oncology
- Experience in early development and transition from FIH to registrational trials
- Both large and small company experience
What you get
- Paid Time Off, Holiday, and Sick Leave
- Medical, Dental and Vision Plans
- Short- and Long-Term Disability
- Basic and Voluntary Life/AD&D Coverage
- Flexible Spending Accounts (FSA, HSA, and Commute)
- Critical Illness and Accident Coverage
Worth weighing
- No specific mention of remote work flexibility beyond location options
- Salary range provided but may vary based on experience and other factors
- Role involves significant responsibilities in a fast-paced environment
Summarised from Erasca's posting. Read the full original.
Listed by Erasca on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
More roles at Erasca
- Assoc Director, Quality Assurance GMPSouth San Francisco, CA; San Diego, CA; remote