Exel
Patient Recruitment & Retention Strategy & ICF Governance Director (Biotech / Oncology)
Alameda, CA · Director
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About the role
- The responsibilities of this role are executed across all programs, phases and therapeutic areas in clinical trials at Exelixis.
- The base pay range for this position is $164,500 - $234,500 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.
Responsibilities
- Partners cross-functionally and with study teams to execute the methodology for delivering the portfolio of studies within the defined budgets and timelines. This includes, but is not limited to
- Lead informed consent cross-functional governance team and informed consent reviews.
- Maintain ICH/GCP compliance, ensuring quality in every element of our informed consent process and forms.
- Collaborate with Study Delivery Leads to ensure timelines are met.
- Work with internal and external stakeholders to develop tactics in reaching recruitment and retention goals, including more patient friendly study documents.
- Develop a repository of information gathered from informed consent global submissions to integrate into updated templates in an effort to expedite study timelines.
- Support Exelixis Public Relations and external corporate giving, or Employee Resource Group (ERG) initiatives (e.g., community service).
- Performs other duties as assigned
Requirements
- 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.
- BS/BA degree in Science, Business or related discipline and a minimum of 13 years of related experience
- MS/MA degree in Science, Business or related discipline and a minimum of 11 years of related experience
Skills
- BS/BA degree in Science, Business or related discipline and a minimum of 13 years of related experience; or,
- MS/MA degree in Science, Business or related discipline and a minimum of 11 years of related experience; or,
- Equivalent combination of education and experience.
- May require certification in assigned area.
- Typically requires at least 6 years of experience in global informed consent process and forms.
- Experience across different tumor indications and clinical trial phases.
- Experience in electronic data management.
- Experience reducing both patient and site burden during clinical trials.
- Leadership and collaboration in complex matrix run organizations.
- Ability to think through, provide solutions and innovate to recruit and retain participants for clinical trials.
- Knowledge of GCP and regulatory requirements related to conducting clinical trials worldwide.
Compensation
- The base pay range for this position is $164,500 - $234,500 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.
Benefits
- Participate in health authority inspections and activities as appropriate.
This listing is sourced directly from Exel's careers page and normalized into a canonical job model.