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Pharmacovigilance Associate Jobs (NOW HIRING)

Formation Bio

Associate Director, Pharmacology

Boston, NY · On-site

$177K - $232K/yr

About the Position Formation Bio is seeking an Associate Director, Pharmacology to join our Development team. In this role, you will help shape and execute pharmacology strategy across development ...

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How much do pharmacovigilance associate jobs pay per hour?

As of Sep 5, 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 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.

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.

Is pharmacovigilance a good career path?

Pharmacovigilance is a growing field that involves monitoring the safety of pharmaceutical products, with roles like Pharmacovigilance Associate focusing on adverse event reporting and data analysis. It offers opportunities for career advancement, requires attention to detail, and often involves working with regulatory guidelines and safety databases. Many professionals find it a stable and rewarding career in the healthcare and pharmaceutical industries.

What qualifications do I need for pharmacovigilance?

A pharmacovigilance associate typically needs a bachelor's degree in pharmacy, medicine, life sciences, or a related field. Relevant skills include knowledge of drug safety regulations, data analysis, and experience with safety databases or case management tools; certifications such as the Drug Safety Certification (DSC) 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 1% As Needed, 70% Full Time, 27% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $102,217 per year, or $49.1 per hour.

Associate Director, Clinical Pharmacology

Latigo Biotherapeutics

San Francisco, CA • On-site

Full-time

Re-posted 28 days ago

Job description

Title: Associate Director, Clinical Pharmacology


Location:Thousand Oaks, CA or San Francisco, CA


Company Description:

Latigo Biotherapeutics, Inc. is a private, early-stage biotechnology company focused on discovering and developing the next generation of non-opioid medicines for pain and pain-related syndromes. Our mission is the development of novel therapies that transform the lives of patients. We have a robust pipeline with programs ranging from preclinical to late phase. The company, whose headquarters is in Thousand Oaks, CA, with a satellite office in San Francisco, CA, has a highly successful management team as well as an experienced Board of Directors. At Latigo, we value honest science, patient-focus, and innovation.


Position Description:

Reporting to the Head of Clinical Pharmacology, the Associate Director, Clinical Pharmacology will work in our clinical development teams, with significant responsibility for the Clinical Pharmacology package of multiple clinical and Pre-IND programs. In this role, you will help formulate clinical pharmacology strategies from the FIH through registration.


Primary Responsibilities:

  • As part of the development team, you will provide expertise in the clinical development of small molecule programs, in particular the design and oversight for clinical pharmacology studies.
  • Lead and manage design and conduct of clinical pharmacology studies of increasing complexity.
  • Analyze, interpret and author documents for clinical submissions, including but not limited to clinical study protocols and reports, Investigator's Brochures, and the clinical pharmacology sections of regulatory submissions.
  • Interact with regulatory agencies (US and ex-US) as needed.
  • You will be accountable for study-to-program level clinical pharmacology aspects of compounds in the discovery to development stage.
  • You will be responsible for oversight and interaction with consultants and vendors assigned to support clinical pharmacology tasks including PK, PKPD, and clinical assay development.

Qualifications and Requirements:

  • PharmD or PhD in a relevant discipline preferred.
  • 8+ years of experience in Clinical Pharmacology supporting early development in a biotech or pharmaceutical organization.
  • Prior, robust clinical pharmacology experience with small molecules is required. Experience in the design and conduct of multiple types of Phase 1 studies (e.g. FIH, DDI, FE, rBA, etc.) preferred.
  • Proficiency with modern PK analysis software (e.g. Phoenix WinNonLin) required.
  • Knowledge of regulatory requirements for clinical pharmacology preferred.
  • Strong interpersonal skills, and ability to influence development program teams.
  • Excellent verbal and written communication skills, and ability to clearly convey complex concepts to technical and non-technical audiences preferred.
  • Ability to work independently in a dynamic and fast-paced environment.
  • Experience in therapeutic areas related to pain management preferred.
  • Experience with regulatory submissions in early and late development is preferred.

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