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Pharmacovigilance Jobs in Bothell, WA (NOW HIRING)

Jobtailor

Director, Pharmacovigilance

Seattle, WA · On-site

$110 - $180/hr

Contribute to development and maintenance of SOPs and Pharmacovigilance System Master File (PSMF) Requirements * Advanced degree (PharmD, PhD, MD, or MS) or health‑related degree/certification (PA ...

micro1 AI

Pharmacovigilance Expert

Renton, WA · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role ...

micro1 AI

Pharmacovigilance Expert

Everett, WA · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role ...

micro1 AI

Pharmacovigilance Expert

Bellevue, WA · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role ...

micro1 AI

Pharmacovigilance Expert

Seattle, WA · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role ...

micro1 AI

Clinical Pharmacy Technicians

Everett, WA · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role ...

micro1 AI

Clinical Pharmacy Technicians

Renton, WA · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role ...

micro1 AI

Clinical Pharmacy Technicians

Bellevue, WA · Remote

$70 - $80/hr

Pharmacovigilance Expert Role Type: Contractor Location: Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role ...

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Pharmacovigilance information

See Bothell, WA salary details

$25

$51

$93

How much do pharmacovigilance jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for pharmacovigilance in Bothell, WA is $51.67, according to ZipRecruiter salary data. Most workers in this role earn between $30.10 and $61.83 per hour, depending on experience, location, and employer.

What is the difference between Pharmacovigilance vs Drug Safety Associate?

AspectPharmacovigilanceDrug Safety Associate
CredentialsTypically requires a degree in pharmacy, life sciences, or related fields; certifications like PV or drug safety training are commonSimilar educational background; often requires training in drug safety and pharmacovigilance practices
Work EnvironmentPharmacovigilance professionals often work in pharmaceutical companies, CROs, or regulatory agencies, focusing on safety data analysisDrug Safety Associates usually work in similar settings, handling case processing and safety reporting
Industry UsageUsed broadly across pharma, biotech, and regulatory sectors for safety monitoringPrimarily used within pharmaceutical companies and CROs for case management and reporting

Both roles focus on drug safety, with pharmacovigilance encompassing a broader scope of safety monitoring, analysis, and regulatory compliance, while Drug Safety Associates typically handle case processing and reporting tasks within that framework.

What are pharmacovigilance jobs?

Pharmacovigilance positions may include a drug safety associate, drug safety scientist, drug safety manager or director, pharmaceutical information specialist, and related positions such as administrative positions and technical writers who specialize in pharmacovigilance writing. The duties of drug safety scientists and associates are to perform research, monitor trials, and investigate adverse effect reports. Information specialists record, categorize and store data related to drugs. Pharmacovigilance directors oversee pharmacovigilance operations, communicate with physicians, drug makers, and regulators when necessary, and ensure compliance with regulations.

Is pharmacovigilance a good career?

Pharmacovigilance is a growing field that involves monitoring the safety of pharmaceutical products, requiring skills in data analysis and regulatory compliance. It offers opportunities in the pharmaceutical and healthcare industries, with roles often requiring certifications and attention to detail. The career can be stable and rewarding for those interested in drug safety and public health.

What kind of job is pharmacovigilance?

Pharmacovigilance is a field focused on detecting, assessing, and preventing adverse effects of pharmaceutical products. Professionals in this area analyze safety data, prepare reports, and ensure compliance with regulatory requirements, often using specialized software and requiring knowledge of drug safety regulations. It is essential for maintaining medication safety and public health.

What is pharmacovigilance?

Pharmacovigilance is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. It plays a crucial role in ensuring the safety and efficacy of medicines once they are released on the market. Professionals in pharmacovigilance monitor reports of side effects and work with healthcare providers, regulatory agencies, and pharmaceutical companies to minimize risks to patients. This field helps maintain public health by identifying potential issues with medications and recommending actions such as warnings, restrictions, or even withdrawal of drugs if necessary.

How much do pharmacovigilance jobs pay in the US?

Pharmacovigilance jobs in the US typically offer salaries ranging from $70,000 to $120,000 annually, depending on experience, education, and location. Entry-level positions may start around $60,000, while senior roles with specialized skills or certifications can exceed $130,000.

What are some common challenges faced by professionals in pharmacovigilance, and how can they be addressed?

Pharmacovigilance professionals often encounter challenges such as managing large volumes of safety data, staying updated with evolving global regulations, and ensuring clear communication across multidisciplinary teams. Addressing these challenges typically involves continuous training, leveraging advanced data management tools, and fostering strong collaboration with regulatory, clinical, and medical affairs teams. Proactively engaging in professional development and adopting best practices in data analysis and reporting can also help professionals navigate these complexities effectively.
More about Pharmacovigilance jobs
What are the most commonly searched types of Pharmacovigilance jobs in Bothell, WA? The most popular types of Pharmacovigilance jobs in Bothell, WA are:
What are popular job titles related to Pharmacovigilance jobs in Bothell, WA? For Pharmacovigilance jobs in Bothell, WA, the most frequently searched job titles are:
What job categories do people searching Pharmacovigilance jobs in Bothell, WA look for? The top searched job categories for Pharmacovigilance jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Pharmacovigilance jobs? Cities near Bothell, WA with the most Pharmacovigilance job openings:
Pharmacovigilance jobs near you
Infographic showing various Pharmacovigilance job openings in Bothell, WA as of July 2026, with employment types broken down into 80% Full Time, and 20% Contract. Highlights an 79% In-person, and 21% Remote job distribution, with an average salary of $107,479 per year, or $51.7 per hour.

Director, Pharmacovigilance

Umoja Biopharma

Seattle, WA

Full-time

Re-posted 8 days ago

Job description

Umoja Biopharma is an industry-leading biotech with locations in Seattle, WA and Louisville, CO, focused on transforming the treatment of cancer with a novel integrated immunotherapy platform. Our vision is to develop off-the-shelf therapies capable of treating any tumor, any time. We are a diverse and growing team working in brand-new facilities in downtown Seattle, Washington and Louisville, Colorado, and we are looking for innovative thinkers who are excited by groundbreaking science and technology, and passionate about squaring up to the challenges inherent to cutting-edge drug development. We are committed to our core values and principles that support our overall mission and strongly invite applications from enthusiastic individuals who share our commitment and help position Umoja to deliver on our goals. We at Umoja believe in the importance of stories; we are looking for great people to join our team to help us create more stories for ourselves, for you, and most importantly for patients and their families.

Umoja Biopharma – Your Body. Your Hope. Your Cure.

POSITION SUMMARY:

The Director of Pharmacovigilance (PV) will play a critical role in executing Umoja Biopharma's global safety strategy across clinical-stage programs. This individual will be responsible for day-to-day pharmacovigilance operations, ensuring high-quality safety data management, regulatory compliance, and effective signal detection.

Working cross-functionally with Clinical Development, Regulatory, and external partners, the Director will help build and optimize scalable PV processes to support Umoja's advancing pipeline, with an emphasis on operational excellence and inspection readiness.

This role will operate as an Individual Contributor and manage PV relationships with vendors and CROs to start. This person may be responsible for building the Pharmacovigilance team and organization in Umoja in the near future.

This position will ideally be based out of our Seattle, WA office and work onsite at least 2 days/week. This position may have the ability to be remote in the US based on candidate experience.

CORE ACCOUNTABILITIES:

Pharmacovigilance Operations

  • Oversee case processing activities, including intake, triage, medical review support, and expedited reporting
  • Ensure compliance with global safety reporting requirements (FDA, EMA, ICH guidelines)
  • Manage relationships with PV vendors/CROs, ensuring service quality, timeliness, and data integrity
  • Support maintenance of safety databases and related systems (e.g., Argus, ArisGlobal)
  • Coordinate with Clinical Development to drive internal cross-functional pharmacovigilance activities

Aggregate Reporting & Regulatory Support

  • Lead or contribute to preparation of DSURs, PSURs/PBRERs, and IND safety reports
  • Support safety sections of regulatory submissions and responses to health authority queries
  • Contribute to development and maintenance of SOPs and Pharmacovigilance System Master File (PSMF)

Signal Detection & Risk Management

  • Support signal detection activities, including data review, trend analysis, and documentation
  • Participate in safety review meetings and cross-functional risk discussions
  • Assist in development and implementation of Risk Management Plans (RMPs)

Cross-Functional Collaboration

  • Partner with Clinical Development on protocol safety design, adverse event monitoring, and investigator communications
  • Collaborate with Regulatory Affairs to ensure alignment on safety reporting strategy
  • Support Medical Affairs in communicating safety information as needed

Inspection Readiness & Quality

  • Ensure PV processes are audit- and inspection-ready
  • Participate in internal audits, vendor audits, and regulatory inspections
  • Drive continuous improvement initiatives across PV operations

The successful candidate will have:

Education & Experience

  • Advanced degree (PharmD, PhD, MD, or MS) or health-related degree/certification (PA, RN, NP)) with at least 10 years of pharmacovigilance experience in biotech or pharmaceutical industry is required
  • Experience supporting clinical-stage programs and working with outsourced PV models
  • Exposure to regulatory submissions and inspections preferred

Technical Expertise

  • Strong working knowledge of global pharmacovigilance regulations (FDA, EMA, ICH)
  • Experience with safety databases and case processing workflows
  • Familiarity with aggregate reporting and signal detection processes
  • Experience in oncology, cell therapy, or gene therapy preferred

Leadership & Operating Style

  • Strong execution focus with attention to detail and quality
  • Ability to manage external partners and influence cross-functional teams
  • Comfortable operating in a fast-paced, evolving biotech environment
  • Proactive problem-solver with sound judgment

Physical Requirements:

  • The ideal candidate will be able to work onsite based out of our Seattle, WA office at least 2 days/week. There may be the ability to work remotely within the US and travel to Seattle, WA at least 5 days/month.
  • Ability to travel as needed
  • Ability to sit for prolonged periods of time

Salary Range: $204,000 - $305,000

Benefits Offerings

Umoja Biopharma offers its employees competitive Medical, Dental, and Vision plans. Additionally, we offer Umojians access to a 401k plan through Fidelity, with a 100% match up to their first 4% deferral. Umoja also provides a generous Paid Time Off policy, employee commuter benefits, and cell phone stipend. For a full breakdown of our benefits offerings, please see the Benefits section of our website.