New · posted Nov 1
Exelixis · Biotechnology
Clinical Science Director
- Alameda, CA
- Hybrid
- Full-time
- Director
The role
SUMMARY/JOB PURPOSE
In collaboration with clinical and project teams of the company, the Clinical Science Director designs, plans and develops studies in early and/or late phase clinical oncology. Prepares and authors clinical development related documents including study synopses and protocols. Summarizes study results for preparation of documents and publications. Supports project teams with scientific information and provides progress updates related to the assigned clinical studies.
JOB COMPLEXITY
- Works on complex problems where analysis of situations or data requires an in-depth evaluation of various factors.
- Exercises judgment within broadly defined practices and policies in selecting methods, techniques, and evaluation of criteria for obtaining results.
- Uses professional concepts and company’s policies and procedures to solve a wide range of difficult problems in imaginative and practical ways.
- Networks with key contacts outside own area of expertise.
What you need
Education/Experience
- Pharm.D., PhD, or M.D. and a minimum of 8 years of related experience; or,
- Equivalent combination of education and experience.
Knowledge/Skills
- Comprehensive and detailed knowledge of clinical trial implementation and drug development process.
- Experience in the design, execution, and reporting of clinical trials in oncology with small and large molecule drug candidates.
- Identifies and implements methods and procedures to achieve results with high quality.
- Performs a variety of complicated tasks with a wide degree of creativity and latitude.
- Has complete understanding and wide application of technical principles, theories, concepts, and techniques.
- May lead or manage the work of others by providing guidance to subordinates or teams based on organizational goals and company policy, with responsibility for results, including costs, methods, and staffing.
- Applies strong analytical and business communication skills.
- Highly organized and able to work under tight timelines
- Good public speaking and presentation skills
Experience/The Ideal for Successful Entry into Jobnice to have
- 5-8 years of clinical development experience in the biotechnology or pharmaceutical industry or the equivalent combination of academia and industry.
- Participated in clinical oncology studies with molecular targeted or immunological therapies.
What you'll do
- In collaboration with the clinical study teams for a specific product candidate in clinical development, designs, prepares and initiates study protocols and other required documentation in compliance with project plans, federal regulations, GCP and good medical practice.
- Interacts with investigators and thought leaders in oncology to facilitate the design of clinical synopses and protocols.
- Researches and assists in the selection of investigators for clinical studies.
- Conducts appropriate literature research for the assigned clinical product candidate.
- Collaborates with clinical operations and other internal study team members to develop Informed Consent Forms, Case Report Forms, and CRF instructions.
- May act as contact of the clinical study team for medical monitor inquiries with guidance and oversight of the Medical Monitor assigned to the clinical program.
- Collaborates with clinical operations and other team members in the development of agendas, training materials, and presentation for site visits, investigator meetings, and other study related venues
- Participates in internal safety meetings, analyzes, and reports potential safety events.
- Collaborates with team members in clinical review and interpretation of study data in support for preparation of reports for health authorities including regulatory filing documentation and study close-out reports.
- Contributes to the writing and/or review product specific abstracts, publications, and supports the development of presentations for scientific meetings.
- Provides feedback on emerging clinical and competitive trends.
- Coordinates and facilitates clinical oncology studies by developing and maintaining excellent working relationships with study investigators.
- Delivers high quality scientific presentations on Exelixis investigational agents to physicians and other key external customers.
- Provides clinical education support for internal Exelixis customers.
- Maintains clinical and technical expertise in the therapeutic area of Oncology.
Supervisory Responsibilities
- None
Pay and benefits
$219,000 – $277,500 a year
Employer provided401k plan with company contributions
Group medical, dental and vision coverage
Life and disability insurance
Discretionary annual bonus
Employee stock purchase and long-term incentives
15 vacation days and 17 paid holidays
Where you'll work
Alameda, CAHybridOpen in Maps (opens in a new tab)
More jobs in Alameda, CAWorking conditions
- 10-25% travel requirement.
Location: Alameda, CA Range for this position: $219,000 - $277,500 The base pay offered will take into account job-related knowledge, skills, experience and internal equity, among other factors.In addition to the base salary, as part of our Total Rewards program, Exelixis offers comprehensive employee benefits package, including a 401k plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Employees are also eligible for a discretionary annual bonus program, or if field sales staff, a sales-based incentive plan. Exelixis also offers employees the opportunity to purchase company stock, and receive long-term incentives, 15 accrued vacation days in their first year, 17 paid holidays including a company-wide winter shutdown in December, and up to 10 sick days throughout the calendar year.
If you have a disability and need an accommodation in relation to the recruiting process, please email us at: [email protected].
Our office is a modern space that fosters collaboration and creativity. Teams work closely together, sharing ideas and solutions in a supportive atmosphere. We provide all necessary equipment, including dual monitors and ergonomic chairs, to ensure a comfortable workspace.
Equal opportunity, accessibility and legal noticesExelixis's statements, word for word
DISCLAIMER
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.
We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.
Job intelligence
The context around this role
Live data · November 1, 2026
Salary intelligence
How the pay compares
This role's midpoint is 17% below the US median for Clinical Development roles at this level.
This roleEmployer provided
Director roles in California41 roles publishing pay
Director roles in the US204 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $219,000 | — | $277,500 |
| California (middle half) | $244,000 | $289,000 | $318,500 |
| All US (middle half) | $259,125 | $300,000 | $335,500 |
This role: Exelixis's own published range. Comparisons: the base pay employers published on open Clinical Development roles at the same level on Regulatory Jobs, November 1, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Development
The general path across 263 open Clinical Development roles on Regulatory Jobs, with the titles they carry most. Not Exelixis's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 34 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct11
- Collaboration and leadership10
- Documentation and SOPs8
- Investigations and CAPA5
- Lab testing and methods4
- GMP and compliance1
- Regulatory submissions1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
Exelixis on Regulatory Jobs
- 20
- Open roles
- 20
- Distinct roles
- 2
- Locations
By discipline
- Clinical12 60%
- Quality5 25%
- Regulatory3 15%
By level
- Director15 75%
- Manager2 10%
- VP & Executive1 5%
More roles at Exelixis
- View role
Senior Medical Director, Clinical Development
Alameda, CA · HybridDirectorBiotechnology$351K–$444K
- View role
Clinical Development Medical Director (Biotechnology / Oncology)
Remote, USDirectorBiotechnology$255K–$361K
- View role
Clinical Operations Compliance Director (Biotechnology Oncology)
Remote, USDirectorBiotechnology$180K–$256K
- View role
Senior Director, Clinical Operations (Biotech, Oncology)
Alameda, CADirectorBiotechnology$246K–$350K
Similar Clinical Development roles elsewhere
- View role
Executive Director, Clinical Development
Travere TherapeuticsSan Diego, CA · HybridDirectorBiotechnology$246K–$332K
- View role
Medical Director, Clinical Trial Physician - Neurology
Thermo Fisher ScientificRemote, USDirectorBiotechnologySalary not listed
- View role
Medical Director/Clinical Trial Physician (Rheumatology) - FSP
Thermo Fisher ScientificRemote, US) - North CarolinaDirectorBiotechnologySalary not listed
- View role
Medical Director, Clinical Development, Oncology (Lung, Breast, Colorectal, Gastric Cancers)
RegeneronTarrytown, NYDirectorBiotechnology$285K–$386K
Clinical Science Director at Exelixis
Open until filled. $219K–$278K a year, employer provided.