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$12

$49

$85

How much do pharmacovigilance associate jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for 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 are the typical daily responsibilities of a Pharmacovigilance Associate?

A Pharmacovigilance Associate is responsible for collecting, reviewing, and processing reports of adverse drug reactions, ensuring that all data is accurate and submitted in accordance with regulatory timelines. On a daily basis, you may enter case information into specialized safety databases, conduct follow-ups with healthcare professionals or patients for additional details, and assist in preparing safety reports for regulatory authorities. The role often involves close collaboration with medical, regulatory, and quality assurance teams to support comprehensive drug safety monitoring. You may also participate in ongoing training or audits to maintain compliance with evolving industry standards.

What do pharmacovigilance associates do?

Pharmacovigilance associates monitor, collect, and analyze data on adverse drug reactions and medication safety. They review reports, ensure compliance with regulatory requirements, and support risk management activities using databases and safety tools. Their work helps ensure the safety of pharmaceutical products throughout their lifecycle.

What are the key skills and qualifications needed to thrive in the Pharmacovigilance Associate position, and why are they important?

To thrive as a Pharmacovigilance Associate, you need a strong background in life sciences or pharmacy, attention to detail, and a solid understanding of drug safety regulations. Familiarity with safety databases such as Argus or ARISg, as well as knowledge of global regulatory guidelines like FDA and EMA requirements, is often required. Strong analytical thinking, effective communication, and organizational skills help you manage case reports and collaborate with cross-functional teams. These skills are essential for accurately assessing and reporting adverse drug reactions to ensure patient safety and regulatory compliance.

What is a Pharmacovigilance Associate job?

A Pharmacovigilance Associate is responsible for monitoring, collecting, assessing, and reporting adverse drug reactions (ADRs) to ensure patient safety. They work with regulatory authorities, healthcare professionals, and pharmaceutical companies to analyze drug safety data. Their duties include case processing, literature screening, signal detection, and ensuring compliance with pharmacovigilance regulations. This role is vital for minimizing drug-related risks and maintaining regulatory compliance.

What is the average salary for a pharmacovigilance Associate?

The average salary for a pharmacovigilance associate in the US typically ranges from $60,000 to $80,000 per year, depending on experience, location, and certifications. Entry-level positions may start lower, while experienced professionals with specialized skills can earn higher salaries, often with opportunities for bonuses and benefits.

What skills are required for a pharmacovigilance associate position?

A pharmacovigilance associate needs strong attention to detail, good communication skills, and knowledge of regulatory guidelines such as ICH and GVP. Proficiency in data management tools, medical terminology, and basic understanding of drug safety processes are also essential. Often, a background in life sciences or pharmacy is required, along with the ability to work in a regulated environment.

Is pharmacovigilance a good career?

Pharmacovigilance is a growing field that involves monitoring the safety of pharmaceutical products, making it a stable career option with demand in the healthcare and pharmaceutical industries. It requires attention to detail, knowledge of regulatory guidelines, and often involves working with safety databases and reporting tools. Many professionals find it a rewarding career due to its impact on public health and opportunities for specialization and advancement.
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Pharmacovigilance Associate jobs near you
Infographic showing various Pharmacovigilance Associate job openings in the United States as of June 2026, with employment types broken down into 3% As Needed, 94% Part Time, and 3% Contract. Highlights an 80% Physical, 4% Hybrid, and 16% 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 Inc.

San Rafael, CA

Full-time

Posted 4 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.

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