Clinical Science Director – Biotech Oncology

Exelixis

. Design, plan, and develop early- and/or late-phase clinical oncology studies .

Posted 9/23/2026full-timeRemote • California • United StatesLead💰 $101 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive expertise in clinical oncology study design, execution, and reporting, with a strong focus on compliance with federal regulations and GCP. Possesses advanced analytical skills and the ability to effectively communicate scientific information to diverse audiences.

Highest-signal resume keywords

Clinical Development ExperienceOncology Study DesignRegulatory ComplianceAnalytical SkillsPublic Speaking

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ImplementationStudy Protocol DevelopmentData InterpretationLiterature ResearchClinical Document AuthoringMolecular Targeted TherapiesImmunological TherapiesStudy Results SummarizationSafety Event AnalysisClinical Education Support

Soft Skills

Highly OrganizedBusiness CommunicationPresentation Skills

Tools & Technologies

Informed Consent FormsCase Report FormsCRF Instructions

Certifications & Qualifications

Pharm.D.PhDM.D.

Industry Keywords

BiotechnologyPharmaceutical IndustryClinical OncologyDrug Development ProcessClinical Trials

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Design, plan, and develop early- and/or late-phase clinical oncology studies
Prepare and author clinical development documents, including study synopses and protocols
Summarize study results for documents and publications
Support project teams with scientific information and provide progress updates on assigned studies
Design, prepare, and initiate study protocols and required documentation in compliance with project plans, federal regulations, GCP, and good medical practice
Interact with oncology investigators and thought leaders to facilitate clinical synopses and protocols
Research and assist with investigator selection
Conduct literature research for assigned clinical product candidates
Collaborate on Informed Consent Forms, Case Report Forms, and CRF instructions
Support medical monitor inquiries with guidance and oversight
Develop agendas, training materials, and presentations for site visits and investigator meetings
Participate in internal safety meetings and analyze and report potential safety events
Review and interpret study data for health authority reports, regulatory filings, and study close-out reports
Write and/or review product-specific abstracts and publications and support scientific meeting presentations
Provide feedback on emerging clinical and competitive trends
Coordinate and facilitate clinical oncology studies and maintain relationships with investigators
Deliver scientific presentations on Exelixis investigational agents to physicians and external customers
Provide clinical education support for internal Exelixis customers
Maintain clinical and technical oncology expertise

Requirements

What you’ll need

Pharm.D., PhD, or M.D. and a minimum of 8 years of related experience; or equivalent combination of education and experience
5-8 years of clinical development experience in the biotechnology or pharmaceutical industry or equivalent combination of academia and industry
Participation in clinical oncology studies with molecular targeted or immunological therapies
Comprehensive and detailed knowledge of clinical trial implementation and drug development process
Experience designing, executing, and reporting clinical trials in oncology with small and large molecule drug candidates
Strong analytical and business communication skills
Highly organized and able to work under tight timelines
Good public speaking and presentation skills
Ability to travel 10-25%

Benefits

Comp & perks

401k plan with generous company contributions
Group medical, dental and vision coverage
Life and disability insurance
Flexible spending accounts
Discretionary annual bonus program
Opportunity to purchase company stock
Long-term incentives
15 accrued vacation days in the first year
17 paid holidays including a company-wide winter shutdown in December
Up to 10 sick days throughout the calendar year
Necessary equipment, including dual monitors and ergonomic chairs