Exelixis Inc Posted October 5, 2026

Drug Safety Associate III

Remote, United States Full time
Pharmacovigilance Associate
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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:

This role is responsible for providing Drug Safety expertise and ensuring the quality documentation of safety data, particularly serious adverse events (SAEs).  This role provides support for all major tasks and oversight of outsourced vendors, related to the management and best utilization of case processing activities in the Argus Safety Database, ensuring compliance with global clinical safety and pharmacovigilance regulations and Global Patient Safety department procedures in all aspects of drug safety case processing and reporting.

This role provides support and oversight of all aspects of drug safety study operational activities from study start up to close out.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

Technical duties include but are not limited to:

Processing and assessing SAEs from receipt at Exelixis to case closure in the Argus database, including query generation, narrative, and ASE writing.

MedDRA coding of SAEs and AEs as reported in source documents of SAE reports and development/revision of Exelixis MedDRA Coding Conventions to ensure consistent data categorization.

Defining and applying a high standard of case quality review to ensure sound medical safety data documentation with the support of the Drug Safety Physician.

Scheduling submissions of expedited safety reports in ARGUS as needed.

Training of new safety staff on Argus and case processing.

Collaborating with other Exelixis departments (Clinical Development, Clinical Operations, Data Management, Regulatory Affairs, Project Management) to ensure appropriate collection and handling of safety data.

Performing Safety Study Lead activities including: Review of, Investigator Brochures, study protocols and participation on IND Annual Reports in support of the Drug Safety Physician.

Development of study specific safety management plan from Exelixis Drug Safety template

Development, review and update of drug safety forms and templates, and harmonization with relevant clinical operation forms and templates (i.e., SAE data collection form and CRF)

Perform SAE reconciliation, as required by safety management plan.

Additional duties and responsibilities as required.

SUPERVISORY RESPONSIBILITIES:

None

EDUCATION/EXPERIENCE/KNOWLEDGE & SKILLS:

Education/Experience:

BS/BA degree in Nursing, Pharmacy, other clinical, or related discipline and a minimum of 7 years of related experience; or,

MS/MA degree in Nursing, Pharmacy, other clinical, or related discipline and a minimum of 5 years of related experience; or,

PhD in Nursing, Pharmacy, other clinical, or related discipline and 0 or more years of related experience; or,

Equivalent combination of education and experience.

May require certification in assigned area.

Experience/The Ideal for Successful Entry into Job:

Experience in Biotech/Pharmaceutical industry and/or in oncology preferred.

Experience using Argus safety database preferred.

Clinical trial and spontaneous adverse event processing experience.

Knowledge/Skills:

Knowledge of biotechnology/pharmaceutical sector.

Knowledge of regulatory framework governing patient safety.

Adopts an analytical approach to solve problems relevant to the role.

Demonstrates an understanding of organizational and planning capabilities by managing own time and resources to complete assigned work.

Leads self by managing and executing own work to deliver results that contribute to accomplishing common departmental goals.

Provides verbal and written communications that are clear and easy to understand. Keeps management informed of potential issues in a timely manner.

Works collaboratively with team members.

Good interpersonal skills, understanding of differing views and participation in developing agreed upon resolution.

Trains on procedures, tasks and tools for role, supported by ongoing coaching and/or mentoring by departmental peers. Develops and maintains knowledge of cross-functional products, tools and data sources. May mentor junior team members.

JOB COMPLEXITY:

Capable of following predefined procedures for specific tasks.

Capable of identifying task-related challenges and prioritizing activity accordingly.

Identifies and escalates issues that may have a broader impact.

Implements solutions to address any task-related challenges.

#LI-JP1

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 $130,500 - $185,000 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
Associate
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 31 comparable Associate Pharmacovigilance roles across 22 biopharma companies.

31Comparable roles tracked
29Currently active
22Companies hiring similar roles
16Countries represented

Salary context

1 of 31 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 $130,500/yr – $185,000/yr
Only peer reporting · Drug Safety Associate II · Exelixis Inc $104,500/yr – $148,000/yr
Peer group range $126,250 – $126,250 (median $126,250)

Where these roles are based

Top locations among the 31 comparable roles

United States7
India5
France4
Japan2
Germany2
Costa Rica1

+ 10 more countries

Seniority mix

31 of 31 peers have a known seniority level

Manager21
Intern/Fellow/Postdoc6
Associate4

Therapeutic area mix

1 of 31 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology1

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
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Same function Same seniority Same country
50%similar
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50%similar
Amgen Inc. Remote, United States Manager
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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%
Drug Safety Associate II
Exelixis Inc · Alameda, United States · Associate
Function Therapeutic area Seniority Country
50%
Global Pharmacovigilance (PV) Scientist, Manager- Oncology
Amgen Inc. · Remote, United States · Manager
Function Therapeutic area Adjacent seniority Country
45%
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BMS Services Sp. z o.o. · Warsaw, Poland · Associate
Function Therapeutic area Seniority Country
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GSK Life Sciences FZE · Uae, United Arab Emirates · Associate
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.