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Pharmacovigilance Associate Jobs (NOW HIRING)

ConnectiveRx

Specialist, Pharmacovigilance

Whippany, NJ

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Assists Pharmacovigilance teammates with tasks such as periodic reconciliation, records inspection ... Associate degree or professional diploma in healthcare, pharmacy, or a medical-related field, or ...

Gilead

Associate Clinical Pharmacology Director

Parsippany, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

We are looking for an Associate Director, Clinical Pharmacology based in our Foster City, CA office or Parsippany, NJ office, supporting drug development in Virology, Pediatrics therapeutic areas. We ...

Gilead

Associate Clinical Pharmacology Director

Parsippany, NJ · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

We are looking for an Associate Director, Clinical Pharmacology based in our Foster City, CA office or Parsippany, NJ office, supporting drug development in Virology, Pediatrics therapeutic areas. We ...

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How much do pharmacovigilance associate jobs pay per hour?

As of Aug 14, 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 are the key skills and qualifications needed to thrive as a pharmacovigilance associate?

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?

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.

How much do pharmacovigilance associates make in the US?

Pharmacovigilance associates in the US typically earn between $60,000 and $85,000 annually, depending on experience, location, and certifications. Entry-level positions may start around $50,000, while experienced professionals with specialized skills can earn higher salaries. The role often requires knowledge of safety databases and regulatory guidelines such as ICH and FDA standards.

Is pharmacovigilance a good career path?

Pharmacovigilance is a growing field that involves monitoring the safety of pharmaceutical products, making it a stable career option for those interested in healthcare and drug safety. It typically requires attention to detail, knowledge of medical terminology, and familiarity with regulatory guidelines, with roles often involving data analysis and report writing. The demand for pharmacovigilance associates is expected to increase as drug development and safety monitoring become more complex.

What is the role of a pharmacovigilance associate?

A pharmacovigilance associate is responsible for monitoring, collecting, and analyzing adverse drug reaction reports to ensure medication safety. They review safety data, prepare reports for regulatory authorities, and support compliance with pharmacovigilance regulations using tools like safety databases. Strong attention to detail and knowledge of regulatory guidelines are essential in this role.

How to become a pharmacovigilance associate?

To become a pharmacovigilance associate, candidates typically need a bachelor's degree in pharmacy, life sciences, or a related field. Relevant skills include knowledge of drug safety regulations, data entry, and adverse event reporting, often supported by certifications like the Drug Safety and Pharmacovigilance Certificate. Gaining experience through internships or entry-level roles in healthcare or pharmaceutical companies can also be beneficial.
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Pharmacovigilance Associate jobs near you
Infographic showing various Pharmacovigilance Associate job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, and 13% Contract. Highlights an 79% In-person, and 21% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Senior Manager, Pharmacovigilance

ORIC Pharmaceuticals

San Diego, CA • On-site, Remote

Full-time

Re-posted 18 days ago

Job description

Company Description
ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com, and follow us on X or LinkedIn.
The Senior Manager of Pharmacovigilance will be responsible for the execution of global pharmacovigilance activities supporting late-stage clinical development and preparation for first commercial launch of small-molecule oncology products in lung and prostate cancer. This role will ensure compliance with global safety regulations and will work closely with cross-functional partners to ensure individual case safety report (ICSR) processing, Health Authority submissions, and post-marketing safety readiness.
This is a hands-on role well suited for a biotech environment requiring both operational excellence and cross-functional collaboration.
Job Description
Global Drug Safety & Pharmacovigilance Operations
  • Manage end-to-end pharmacovigilance activities for clinical trials and post-approval oncology products
  • In partnership with Clinical Research Organizations (CROs), oversee intake, assessment, processing, medical review, and reporting of ICSRs from clinical trials, adhering to established processes and timelines
  • Ensure timely submission of expedited and periodic safety reports to Regulatory Authorities, IRBs/ECs, clinical investigators, and business partners
  • Support preparation and submission of DSURs, periodic safety reports/listings, and updates to Investigator Brochures (IBs)
  • Develop, maintain and execute Safety Management Plans for clinical studies

Clinical Development & Regulatory Affairs Support
  • Contribute to safety sections of clinical study protocols, informed consent forms (ICFs), clinical study reports (CSRs) and IND/NDA/MAA/CTAs (as applicable)
  • Review clinical trial safety data and assist with data cleaning for ongoing studies
  • Participate in periodic safety reviews, signal detection and risk evaluation activities
  • Maintain Reference Safety Information for ORIC products and co-administered IMPs
  • Support launch readiness activities including development of post-marketing pharmacovigilance processes, development and maintenance of Risk Management Plans (RMPs) and REMS (as applicable)
  • Assist with preparation for regulatory inspections and audits

Cross-Functional Collaboration
  • Participate in internal Safety Management Teams and governance meetings
  • Partner with Clinical, Regulatory Affairs, Medical Affairs, Quality, and Commercial teams
  • Support safety training for internal stakeholders and investigators

Vendor & Compliance Oversight
  • Support oversight of pharmacovigilance vendors and service providers
  • Ensure Safety Data Exchange Agreements (SDEAs) are implemented and maintained
  • Assist in development and maintenance of SOPs and training materials

Qualifications
Required Qualifications
  • Bachelor's degree in life sciences, pharmacy, nursing, or related discipline with demonstrated knowledge of medical terminology
  • 12 years' pharmacovigilance experience with Bachelor's degree -or- 8 years' experience and Master's degree -or- 5 years' experience and PhD-including clinical trial and/or post-marketing experience
  • Experience with small-molecule oncology products
  • Working knowledge of global pharmacovigilance regulations, including FDA, EMA, Health Canada, and Asian Health Authorities (e.g., Japan PMDA, South Korea MFDS)
  • Experience using validated safety databases (e.g., Argus, ARISg) and clinical trial databases

Preferred Qualifications
  • Oncology experience in lung and/or prostate cancer
  • Experience in biotech/ small pharmaceutical company or CRO environments
  • Experience supporting NDA/MAA submissions and commercial launch
  • Familiarity with REMS, RMPs, and post-marketing commitments

Skills and Attributes
  • Strong strategic thinking combined with a hands-on, execution-focused mindset
  • Proven ability to collaborate and lead in a cross-functional, matrixed organization
  • Excellent written and verbal communication skills, with the ability to convey complex data clearly
  • Highly organized, adaptable, and comfortable working in a fast-paced, evolving environment
  • Mission-driven, patient-focused, and committed to scientific integrity

Additional Information
The anticipated salary range for candidates who will work on-site at our San Diego location is between $150,000-$180,000. The final wage offered to a successful candidate will be dependent on several factors that may include, title, type and length of experience within the role, type and length of experience within the industry, education, geography, and other job-related factors. This position is not eligible for H-1B visa sponsorship.
ORIC Pharmaceuticals, Inc. is an equal opportunity employer. ORIC does not discriminate based on race, color, religion, gender, sexual orientation, gender identity, age, national origin, disability status, protected veteran status, or any other legally protected characteristics.

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