Exelixis Visa Sponsorship USA
Exelixis is a clinical-stage oncology company with a consistent track record of sponsoring international talent across research, regulatory, and clinical functions. For foreign nationals targeting a career in biotechnology and pharmaceuticals, Exelixis is a legitimate and active visa sponsor worth pursuing.
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SUMMARY/JOB PURPOSE:
The Executive Medical Director, PVRM is responsible for the development and execution of the global product safety strategy for complex clinical development program(s) as well as post-marketing pharmacovigilance activities for Exelixis products. This role leads and mentors team members to proactively and successfully plan and manage key safety surveillance activities, safety analyses, risk management and safety document deliverables. This role also engages and collaborates cross-functionally to execute on the corporate development strategy.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
The incumbent operates in a matrix environment within the global patient safety function and the broader development organization. Responsibilities for this position include:
- Lead and develop the safety strategy for complex clinical development programs for oncology products in development or products with a marketing authorization.
- Create appropriate safety data analysis strategies across clinical studies for a product.
- Perform appropriate data interpretation on the performed safety analyses for a product.
- Set a clear strategy for key safety deliverables for the product (e.g., safety signals, aggregate reports, risk management planning, safety data pooling, regulatory filing documents, clinical development documents).
- Lead the cross-functional Benefit Risk Team for the assigned product and escalate important safety updates to the Benefit Risk Executive Committee in a timely fashion.
- Lead the development of core safety documents, which characterize the safety profile of the product appropriately.
- Lead proactive safety data reviews and anticipate safety concerns for the assigned product.
- Oversee the development of safety data evaluations and summaries in the global periodic safety aggregate reports for the product.
- Present safety data and provide safety expertise on the product during key meetings (e.g., with Health Authorities, Data Safety Monitoring Boards and Investigators).
- Develop risk management strategies and monitoring plans for risk management effectiveness for the product.
- Co-lead the benefit-risk assessment for the product with other functions.
SUPERVISORY RESPONSIBILITIES:
- Has supervisory responsibilities over direct reports.
- Significant cross-functional and cross-departmental interactions with clinical development, biometrics, medical affairs and regulatory affairs.
EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:
Education/Experience:
- M.D. degree and a minimum of 10 years of post-residency experience; or, equivalent combination of education and experience.
Experience/The Ideal for Successful Entry into Job:
- 3+ years of clinical experience post-residency.
- Board Certification (if US) preferred.
- At least 10 years of experience of pharmacovigilance experience or other relevant experience (e.g., Clinical Research) in a pharmaceutical/biotechnology company.
- Significant clinical experience may compensate for shorter experience in pharmaceutical/biotech company.
- Pharmacovigilance experience in Oncology is a plus.
- Prior project and team leadership/management experience is preferred.
- Solid knowledge and understanding of US and EU pharmacovigilance regulatory requirements and general regulatory expectations.
Knowledge/Skills:
- Extensive knowledge of biotechnology/pharmaceutical sector drivers and practices throughout the entire product lifecycle.
- Extensive knowledge of US and international pharmacovigilance regulations, with experience in their practical application throughout the entire product lifecycle.
- Demonstrates advanced skill and keen insight in gathering, analyzing and applying key information to solve complex problems.
- Demonstrates strong organizational and planning capabilities by managing time, workload and resources of a function.
- Leads and manages a functional area within a department to execute on team functional objectives that contribute to accomplishing common functional and departmental goals.
- Demonstrates high standards of verbal and written communication. Selects communication method and medium appropriate to the message and the audience. Speaks clearly and confidently in one-to-one situations and effectively presents to large audiences within and outside Exelixis.
- Strong interpersonal skills and ability to incorporate differing views to resolve challenges and develop agreed upon resolutions.
- Develops procedures, tasks and tools. Trains staff on departmental products, tools and data sources. Develops and maintains knowledge of cross-functional products, tools and data sources. Mentors junior team members. Contributes to performance reviews and professional development plans of team members.
JOB COMPLEXITY:
- Capable of strategically and proactively assessing workload, trends, tasks and priorities for cross-functional activity.
- Plans and executes multiple projects or activities, considering alternative methods and contingency plans to avoid potential issues and promote efficiency.
- Designs and implements solutions to address cross functional challenges, taking into consideration the broader impact.
WORKING CONDITIONS:
Notice to Recruiters/Staffing Agencies
Recruiters and staffing agencies should not contact Exelixis, Inc. through this page. We require that all recruiters and staffing agencies have a signed contract on file and be assigned a specific search by our human resources department. Any resumes submitted through the website or directly by recruiters or staffing agencies that do not meet the above-mentioned criteria will be considered unsolicited and the company will not be responsible for any related fees.
If you like wild growth and working with happy, enthusiastic over-achievers, you'll enjoy your career with us!
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 $355,000 - $504,000 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.
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.

SUMMARY/JOB PURPOSE:
The Executive Medical Director, PVRM is responsible for the development and execution of the global product safety strategy for complex clinical development program(s) as well as post-marketing pharmacovigilance activities for Exelixis products. This role leads and mentors team members to proactively and successfully plan and manage key safety surveillance activities, safety analyses, risk management and safety document deliverables. This role also engages and collaborates cross-functionally to execute on the corporate development strategy.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
The incumbent operates in a matrix environment within the global patient safety function and the broader development organization. Responsibilities for this position include:
- Lead and develop the safety strategy for complex clinical development programs for oncology products in development or products with a marketing authorization.
- Create appropriate safety data analysis strategies across clinical studies for a product.
- Perform appropriate data interpretation on the performed safety analyses for a product.
- Set a clear strategy for key safety deliverables for the product (e.g., safety signals, aggregate reports, risk management planning, safety data pooling, regulatory filing documents, clinical development documents).
- Lead the cross-functional Benefit Risk Team for the assigned product and escalate important safety updates to the Benefit Risk Executive Committee in a timely fashion.
- Lead the development of core safety documents, which characterize the safety profile of the product appropriately.
- Lead proactive safety data reviews and anticipate safety concerns for the assigned product.
- Oversee the development of safety data evaluations and summaries in the global periodic safety aggregate reports for the product.
- Present safety data and provide safety expertise on the product during key meetings (e.g., with Health Authorities, Data Safety Monitoring Boards and Investigators).
- Develop risk management strategies and monitoring plans for risk management effectiveness for the product.
- Co-lead the benefit-risk assessment for the product with other functions.
SUPERVISORY RESPONSIBILITIES:
- Has supervisory responsibilities over direct reports.
- Significant cross-functional and cross-departmental interactions with clinical development, biometrics, medical affairs and regulatory affairs.
EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:
Education/Experience:
- M.D. degree and a minimum of 10 years of post-residency experience; or, equivalent combination of education and experience.
Experience/The Ideal for Successful Entry into Job:
- 3+ years of clinical experience post-residency.
- Board Certification (if US) preferred.
- At least 10 years of experience of pharmacovigilance experience or other relevant experience (e.g., Clinical Research) in a pharmaceutical/biotechnology company.
- Significant clinical experience may compensate for shorter experience in pharmaceutical/biotech company.
- Pharmacovigilance experience in Oncology is a plus.
- Prior project and team leadership/management experience is preferred.
- Solid knowledge and understanding of US and EU pharmacovigilance regulatory requirements and general regulatory expectations.
Knowledge/Skills:
- Extensive knowledge of biotechnology/pharmaceutical sector drivers and practices throughout the entire product lifecycle.
- Extensive knowledge of US and international pharmacovigilance regulations, with experience in their practical application throughout the entire product lifecycle.
- Demonstrates advanced skill and keen insight in gathering, analyzing and applying key information to solve complex problems.
- Demonstrates strong organizational and planning capabilities by managing time, workload and resources of a function.
- Leads and manages a functional area within a department to execute on team functional objectives that contribute to accomplishing common functional and departmental goals.
- Demonstrates high standards of verbal and written communication. Selects communication method and medium appropriate to the message and the audience. Speaks clearly and confidently in one-to-one situations and effectively presents to large audiences within and outside Exelixis.
- Strong interpersonal skills and ability to incorporate differing views to resolve challenges and develop agreed upon resolutions.
- Develops procedures, tasks and tools. Trains staff on departmental products, tools and data sources. Develops and maintains knowledge of cross-functional products, tools and data sources. Mentors junior team members. Contributes to performance reviews and professional development plans of team members.
JOB COMPLEXITY:
- Capable of strategically and proactively assessing workload, trends, tasks and priorities for cross-functional activity.
- Plans and executes multiple projects or activities, considering alternative methods and contingency plans to avoid potential issues and promote efficiency.
- Designs and implements solutions to address cross functional challenges, taking into consideration the broader impact.
WORKING CONDITIONS:
Notice to Recruiters/Staffing Agencies
Recruiters and staffing agencies should not contact Exelixis, Inc. through this page. We require that all recruiters and staffing agencies have a signed contract on file and be assigned a specific search by our human resources department. Any resumes submitted through the website or directly by recruiters or staffing agencies that do not meet the above-mentioned criteria will be considered unsolicited and the company will not be responsible for any related fees.
If you like wild growth and working with happy, enthusiastic over-achievers, you'll enjoy your career with us!
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 $355,000 - $504,000 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.
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 Roles at Exelixis Companies
How to Get Visa Sponsorship in Exelixis Visa Sponsorship USA
Target roles aligned with drug development
Exelixis's sponsorship activity centers on its core oncology pipeline. Focus your applications on clinical development, regulatory affairs, bioinformatics, and research roles, these functions consistently attract international talent and have the strongest sponsorship precedent.
Green Card pathways are part of the picture
Exelixis has a meaningful history of supporting employees through permanent residency. If long-term U.S. immigration is your goal, ask during the offer stage whether the company has a defined PERM sponsorship policy for your role level.
Apply during peak biotech hiring cycles
Pharmaceutical and biotech companies like Exelixis typically ramp hiring around clinical milestone announcements and fiscal year starts. Timing your application to those windows can improve your chances of finding roles with active headcount and sponsorship budget approved.
Highlight scientific expertise that matches the pipeline
Exelixis's work centers on cabozantinib and oncology combination therapies. Candidates with backgrounds in kinase inhibitors, clinical oncology, or REMS compliance have a natural fit, make that alignment explicit in your application materials to stand out.
Browse verified sponsorship history before applying
Confirming that a company genuinely sponsors before investing time in an application matters. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history, search Exelixis directly to see open roles with confirmed sponsorship activity.
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Get Access To All JobsFrequently Asked Questions
Does Exelixis sponsor H-1B visas?
Yes, Exelixis sponsors H-1B visas. The company has an established pattern of sponsoring foreign nationals in specialty occupation roles, particularly in scientific, clinical, and regulatory functions. If you're applying on H-1B, focus on roles where a degree in a specific field is a stated requirement, Exelixis's hiring tends to reflect that standard.
Which visa types does Exelixis sponsor?
Exelixis sponsors H-1B and TN visas for nonimmigrant work authorization, and supports F-1 OPT candidates in qualifying roles. On the immigrant side, the company has sponsored EB-2 and EB-3 Green Cards, making it a viable long-term option for candidates seeking a path to permanent residency in the U.S.
Which departments or roles at Exelixis are most likely to be sponsored?
Sponsorship at Exelixis is concentrated in roles directly tied to its oncology pipeline, clinical development, regulatory affairs, pharmacovigilance, biostatistics, and translational research are the most common areas. Corporate and commercial roles can be sponsored too, but the highest volume of international hiring typically sits within scientific and medical functions.
How do I find open jobs at Exelixis that offer visa sponsorship?
Migrate Mate is the most efficient way to find Exelixis roles with confirmed sponsorship history. The platform filters by verified sponsors so you're not guessing, search Exelixis by name to surface currently available positions. From there, apply directly and reference your visa type early in your cover letter or outreach.
How do I approach the application timeline when targeting Exelixis as an H-1B or OPT candidate?
If you're on F-1 OPT, apply with enough runway for Exelixis to file an H-1B cap-subject petition before your OPT expires. H-1B cap petitions must be filed by April 1 for an October 1 start, so ideally secure an offer by February or March. TN candidates have more flexibility since TN status can be obtained at the border with an offer letter.
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