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Full Time Pharmacovigilance Associate Jobs (NOW HIRING)

Frontage Laboratories

Associate Scientist

Exton, PA · On-site

Associate Scientist (Pharmacokinetics) - Biologics Location: 760 Pennsylvania Dr, Exton, PA 19341 Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research ...

BioPhase Solutions

Research Associate

Los Angeles, CA · On-site

$25 - $35/hr

The Research Associate, Discovery Biology and Pharmacology is a 6+ months temporary role with a possibility of conversion to full-time in our Research division. The position is in a dynamic and ...

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Full Time Pharmacovigilance Associate information

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How much do full time pharmacovigilance associate jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for full time pharmacovigilance associate in the United States is $49.14, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $55.53 per hour, depending on experience, location, and employer.

What is the difference between Full Time Pharmacovigilance Associate vs Full Time Drug Safety Associate?

AspectFull Time Pharmacovigilance AssociateFull Time Drug Safety Associate
CertificationsTypically requires life sciences degree; certifications like PV training are a plusSimilar requirements; often the same certifications are valued
Work EnvironmentPharmacovigilance departments in pharma or biotech companiesDrug safety teams within pharmaceutical or CRO settings
Employer & Industry UsageCommonly used in pharma, biotech, and CROsOften used interchangeably with pharmacovigilance associate in industry

Both roles involve monitoring drug safety data, reporting adverse events, and ensuring regulatory compliance. The terms are often used interchangeably, with slight variations depending on company terminology. They share similar responsibilities, work environments, and required qualifications, making them closely related positions in the drug safety field.

More about Full Time Pharmacovigilance Associate jobs
What cities are hiring for Full Time Pharmacovigilance Associate jobs? Cities with the most Full Time Pharmacovigilance Associate job openings:
What job categories do people searching Full Time Pharmacovigilance Associate jobs look for? The top searched job categories for Full Time Pharmacovigilance Associate jobs are:
Full Time Pharmacovigilance Associate jobs near you
Infographic showing various Full Time Pharmacovigilance Associate job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 87% In-person, and 13% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.
Pharmacovigilance Associate II

Pharmacovigilance Associate II

BIOMARIN PHARMACEUTICAL

San Rafael, CA • On-site

Full-time

Posted 26 days ago

Job description

Who We Are
BioMarin is a global biotechnology company that relentlessly pursues bold science to translate genetic discoveries into new medicines that advance the future of human health.
Since our founding in 1997, we have applied our scientific expertise in understanding the underlying causes of genetic conditions to create transformative medicines, using a number of treatment modalities.
Using our unparalleled expertise in genetics and molecular biology, we develop medicines for patients with significant unmet medical need. We enlist the best of the best - people with the right technical expertise and a relentless drive to solve real problems - and create an environment that empowers our teams to pursue bold, innovative science. With this distinctive approach to drug discovery, we've produced a diverse pipeline of commercial, clinical and preclinical candidates that have well-understood biology and provide an opportunity to be first-to-market or offer a substantial benefit over existing therapeutic options.
The mission of the Pharmacovigilance (PV) function is to lead multidisciplinary efforts to actively and effectively monitor the safety of Pharmacovigilance products throughout their lifecycle, rapidly act on validated new safety information, and ensure a state of global PV compliance.

Summary
The Associate is responsible for case initiation, data entry for non-expedited ICSRs, quality review and submissions
The Associate II position requires a solid foundational ability to communicate well and work collaboratively on a team and a good level of competence to act proactively and effectively respond to workflow challenges. An aptitude for effective decision-making and problem-solving is also required.
Key Responsibilities:
Case Initiation and Processing
Monitor the BPV Inbox and Argus safety database for receipt of safety information routinely throughout the business day
Promptly review all relevant incoming items, using source document(s) to assess whether the case is valid and checking for duplicate cases; initiate all initial reports into the safety database per appropriate work instruction
Case Initiation and Processing
Monitor the BPV Inbox and Argus safety database for receipt of safety information routinely throughout the business day
Promptly review all relevant incoming items, using source document(s) to assess whether the case is valid and checking for duplicate cases; initiate all initial reports into the safety database per appropriate work instruction
Perform data entry for all non-serious ICSRs and all serious, non-expedited ICSRs (serious ICSRs with no regulatory submissions), ensuring timelines are met
Ensure all pending actions are completed and earliest received cases are prioritized; leverage email classification systems to categorize and prioritize incoming cases
Process follow up cases / previously reported events
Confirm receipt of case information by forwarding confirmation of safety reports received and providing Pharmacovigilance case numbers to appropriate partners
Perform quality review. Review the source documentation to identify data which should be entered into the safety database, including review of all applicable data entered to assure accuracy.
Support submissions, including submitting reports to regulatory authorities and business partners and supporting the development of the cover letter and 1571 form for IND safety reports. Resolve submission problems as necessary.
Conduct reconciliation of vendor / partners safety database with Pharmacovigilance safety database
Education & Experience:
BA/BS degree in health or life sciences. Relevant experience in lieu of education accepted.
3+ years of pharmacovigilance experience


Note: This description is not intended to be all-inclusive, or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned.
Equal Opportunity Employer/Veterans/Disabled
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Employment Type: Fulltime-Regular

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