Oncology Clinical Science Director (Remote)

Exelixis, Inc.; Alameda, Northern (CA, KY); Hybrid; USD 195,000 - 278,000; Full time

Benefits offered by this job

Discretionary annual bonus

Stock purchase plan

Long-term incentives

Vacation: 15 days first year

17 holidays; winter shutdown

Up to 10 sick days

401k plan with contributions

Job summary

Exelixis, Inc. is seeking a Clinical Science Director in Alameda, CA with remote work options. The role designs and develops oncology studies, prepares protocols and synopses, and supports teams with scientific insight.

Expect collaboration with investigators and leadership in publishing and regulatory deliverables. The candidate will contribute to safety reviews, study close-outs, and strategic scientific communications, while maintaining deep therapeutic area expertise in oncology and

Qualifications

• Extensive experience in designing and managing oncology clinical trials.
• Strong knowledge of GCP and regulatory requirements.
• Experience in scientific writing, publication, and presentation.
• Ability to lead cross-functional teams and manage stakeholder expectations.

Responsibilities

• Designs and develops oncology clinical studies across phases.
• Authors study synopses, protocols, and informed consent materials.
• Interacts with investigators and thought leaders to optimize trial design.
• Interprets study data for regulatory filings and publications.
• Delivers scientific presentations to internal and external audiences.

Skills

Clinical trial design & execution

Regulatory knowledge (FDA/GCP)

Medical communication & publication

Team leadership & collaboration

Public speaking & presentation

Education

Pharm.D.

PhD

MD

Job description

Exelixis, Inc. is seeking a Clinical Science Director in Alameda, CA with remote work options. The role designs and develops oncology studies, prepares protocols and synopses, and supports teams with scientific insight.

Expect collaboration with investigators and leadership in publishing and regulatory deliverables. The candidate will contribute to safety reviews, study close-outs, and strategic scientific communications, while maintaining deep therapeutic area expertise in oncology and