Exelixis Inc Posted July 30, 2026

Exec Medical Director, Pharmacovigilance Risk Management (PVRM)

Remote, United States Full time
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Exelixis Inc is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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.

#LI-MB1

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.

If you have a disability and need an accommodation in relation to the recruiting process, please email us at: ApplicantAccommodations@exelixis.com .

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.

Job details

Seniority
Director
Function
Pharmacovigilance
Therapeutic area
Not listed
Location
Remote, United States
Employment type
Full time

How this role compares

Computed from every other active Pharmacovigilance role in our database, not just this employer's listings.

We currently track 23 comparable Director Pharmacovigilance roles across 10 biopharma companies.

23Comparable roles tracked
22Currently active
10Companies hiring similar roles
4Countries represented

Salary context

13 of 23 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $355,000/yr – $504,000/yr
Lowest disclosed · SERM Scientific Director · GlaxoSmithKline LLC $169,950/yr – $283,250/yr
Highest disclosed · Director, Patient Safety (MD) · Gilead Sciences, Inc. $243,100/yr – $314,600/yr
Peer group range $226,600 – $278,850 (median $232,750)

Where these roles are based

Top locations among the 23 comparable roles

United States19
United Kingdom2
Spain1
Canada1

Seniority mix

23 of 23 peers have a known seniority level

Director22
Senior Director1

Therapeutic area mix

8 of 23 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology5
Neuroscience2
Immunology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
AbbVie North Chicago, IL Director
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60%similar
Gilead Sciences, Inc. Foster City, United States Director
Same function Same seniority Same country
60%similar
Celgene - Summit (Corp) Madison, United States Director
Same function Same seniority Same country
60%similar
Celgene - Summit (Corp) Princeton, United States Director
Same function Same seniority Same country
60%similar
E.R. Squibb & Sons,L.L.C. Princeton, United States Director
Same function Same seniority Same country
60%similar
GlaxoSmithKline LLC Durham Blackwell Street, United States Director
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
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Function Therapeutic area Seniority Country
60%
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Otsuka Pharmaceutical Development and Commercialization, Inc. · Princeton, United States · Director
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60%
Senior Medical Director - Patient Safety
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.