COMPANY DESCRIPTION:
Every Exelixis employee is united in an ambitious cause: to launch innovative medicines that give patients, and their families hope for the future. In this pursuit, we know our employees are our most asset. After operating in the challenging biotech sector for 25 years, we have a proven track record of resiliency in the face of adversity. The success of our lead product has provided a solid commercial foundation allowing us to reinvigorate our research efforts and grow our team in areas such as Drug Discovery, Clinical Development and Commercial.
As we expand our global partnerships and further reinvest in R&D to help us discover the next breakthrough for difficult-to-treat cancers, we are seeking to add talented, dedicated employees to power our mission.
Cancer is our cause. Make it yours, too.
SUMMARY/JOB PURPOSE:
Provide strategic scientific leadership for the biologics portfolio across discovery, translational sciences, and early development. Shape and execute biologics research and development strategies aligned with corporate objectives, leveraging deep expertise in antibody drug conjugates (ADCs), antibody therapeutics, protein engineering, multispecifics, and emerging biologic modalities. Partner with cross-functional leaders to identify, evaluate, and advance innovative therapeutic candidates from target selection through clinical proof-of-concept. As a member of the Biotherapeutics team, the Executive Director of Biologics Innovation & Strategy plays a key role in leading the efforts for advancing the development of antibody drug conjugates (ADCs) and other biologics for oncology-based molecules at Exelixis.
The incumbent supports efforts in early development as well as post IND activities of ongoing and new biologics projects.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Develop and lead the scientific strategy for biologics programs across oncology indications, ensuring alignment with corporate R&D objectives and portfolio priorities.
Drive portfolio strategy, including target assessment, modality selection, competitive landscape analysis, and differentiation opportunities.
Serve as a scientific thought leader for biologics innovation, identifying emerging technologies, external trends, and novel therapeutic approaches.
Provide strategic guidance to multidisciplinary teams spanning discovery biology, antibody engineering, protein sciences, translational medicine, CMC, regulatory, and clinical development.
Lead scientific governance discussions and present program recommendations to executive leadership and research review committees.
Evaluate external innovation opportunities, including business development, licensing, academic collaborations, and strategic partnerships.
Influence program direction through interpretation of complex preclinical and translational data, risk-benefit assessments, and development planning.
Establish portfolio-wide scientific frameworks, decision criteria, and stage-gate processes to maximize probability of technical and clinical success.
Represent the organization externally through scientific publications, conference presentations, advisory boards, and interactions with key opinion leaders.
Mentor and develop senior scientific talent, fostering a culture of innovation, collaboration, and scientific excellence.
Project leadership and execution of antibody-based therapeutics programs.
May lead and manage.
Contributor to regulatory filings related to Biotherapeutics molecules including serving as BTX SME on development teams, preparation and writing of IND reports, review and authoring of Pharmacology and adjacent related IND sections.
Superlative Interaction and collaboration skills and communications across multiple departments and functions in both research and development parts of the organization as well as the ability to represent Exelixis with external collaboration colleagues to discuss and resolve project needs and issues in research and development of biotherapeutics.
Supervision of scientific staff.
Follow company intellectual property and compliance policies and practices.
Comply with company health and safety policies and general laboratory practices.
SUPERVISORY RESPONSIBILITIES:
Could supervise staff, including hiring, scheduling, and assigning work, reviewing performance, and recommend salary increases, promotions, transfers, demotions, or terminations.
EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:
Education:
PhD degree in pharmacology or cancer biology or closely related discipline and a minimum of 15 years of related experience; or
Equivalent combination of education and experience.
Experience:
Extensive scientific knowledge of biologics in oncology indications
Research experience with antibody-based therapeutics from discovery to IND.
Expertise in developing and executing on development candidate selection packages and post DC translational strategies for oncology therapeutics.
Broad experience with early biomarker strategies for biologics including ADCs.
Strong background in the biologics domain, including cancer target biology and experience analyzing ‘omics data (such as genomics, proteomics, transcriptomics, and knowledge of relevant databases).
Strong scientific understanding of mechanism of action of cytotoxins and ADCs is essential.
Demonstrated drive for rigorous scientific excellence.
Knowledge/Skills:
Knowledge of state-of-the-art in various aspects of ADC research and development including ADC platforms and applications and a comprehensive understanding of current approaches and emerging technologies in ADCs.
The knowledge to apply advanced scientific and technical principles, theories, and concepts, and contribute to the development of new principles and concepts.
Ability to think critically and strategically with solution-orientated mindset and a hands-on, “roll up your sleeves” approach.
The drive to facilitate, track, anticipate, influence, and implement team objectives; out-of-the-box thinking and willingness to challenge the status quo where relevant.
Ability to work independently, excellent time management and organization skills to manage multiple internal and external projects simultaneously.
Knowledge of intellectual property matters, and issues related to bioconjugates.
Excellent written, oral, and interpersonal communication skills.
WORKING CONDITIONS:
Environment: primarily working in laboratories or in office.
Exposures encountered, such as hazardous materials, extreme cold.
Travel required (10%).
#LI-HG1
Our compensation reflects the cost of labor across several U.S. geographic markets, and we pay differently based on those defined markets. The base pay range for this position is $268,500 - $380,500 annually. The base pay range may take into account the candidate’s geographic region, which will adjust the pay depending on the specific work location. The base pay offered will take into account the candidate’s geographic region, 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].
WORKING CONDITIONS:
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.
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.
Skills Required
- Doctoral degree (Ph.D.) in Pharmacology, Biology, Immunology, Biochemistry, Molecular Biology, Microbiology or related discipline and a minimum of fifteen years industry experience post-Ph.D., or equivalent combination of education and experience
- Strong background in biologics domain with experience in Oncology biologics
- Experience leading and managing Oncology/ADC programs
- Research experience with antibody-based therapeutics from discovery to IND
- Experience writing intellectual property filings, reports, and non-clinical IND sections
- Extensive knowledge of in vitro and in vivo characterization and translational pharmacology of ADCs and bispecifics
- Experience designing, executing, and analyzing in vivo studies to evaluate efficacy, PK/PD, and early toxicology assessments
- Demonstrated ability to supervise, mentor, and expand a Pharm/Tox team and manage internal employees
Exelixis Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Exelixis and has not been reviewed or approved by Exelixis.
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Retirement Support — Retirement plans are highlighted as a strength, featuring a 401(k) with generous company contributions and immediate vesting. This emphasis signals strong long‑term financial support within the total rewards package.
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Healthcare Strength — Healthcare coverage is positioned as comprehensive, with multiple medical plan options (HDHP with HSA, EPO, and Kaiser HMO in CA) and employer HSA contributions in 2026. Posted plan documents and contribution details indicate structured support for managing care and costs.
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Parental & Family Support — Family support is robust, including fully paid parental leave, caregiver leave, and expanded fertility benefits. Additional elements such as grandparent leave and backup care broaden assistance across life stages.
Exelixis Insights
What We Do
Every Exelixis employee is united in an ambitious cause: to launch innovative medicines that give patients and their families hope for the future. In this pursuit, we know our employees are our most valuable asset. After operating in the challenging biotech sector for more than 25 years, we have a proven track record of resiliency in the face of adversity. The success of our lead product has provided a solid commercial foundation allowing us to reinvigorate our research efforts, and grow our team in areas such as Drug Discovery, Clinical Development and Commercial. As we expand our global partnerships and further reinvest in R&D to help us discover the next breakthrough for difficult-to-treat cancers, we’re seeking to add talented, dedicated employees to power our mission. Cancer is our cause. Make it yours, too. Please see our Community Guidelines: bit.ly/2XXw9w3 For more information about Exelixis, please visit www.exelixis.com, follow @ExelixisInc on Twitter or like Exelixis, Inc. on Facebook.








