Responsible for appropriate summarizing and interpreting results of pharmacokinetic/pharmacodynamics analyses with respect to their impact on development and clinical use of drugs. Provides Clinical ...
Responsible for appropriate summarizing and interpreting results of pharmacokinetic/pharmacodynamics analyses with respect to their impact on development and clinical use of drugs. Provides Clinical ...
Senior Manager/Associate Director, Clinical Pharmacology
Princeton, NJ · On-site
$150 - $200/hr
Perform quantitative pharmacology analyses and contribute to the interpretation of study results through all phases of clinical development. * Perform pharmacometric analyses to support drug ...
Senior Manager/Associate Director, Clinical Pharmacology
Princeton, NJ · On-site
$150 - $200/hr
Perform quantitative pharmacology analyses and contribute to the interpretation of study results through all phases of clinical development. * Perform pharmacometric analyses to support drug ...
Senior Manager/Associate Director, Clinical Pharmacology
Princeton, NJ · On-site
$150K - $200K/yr
Perform quantitative pharmacology analyses and contributes to the interpretation of study results through all phases of clinical development. * Perform pharmacometric analyses to support drug ...
Senior Manager/Associate Director, Clinical Pharmacology
Princeton, NJ · On-site
$150K - $200K/yr
Perform quantitative pharmacology analyses and contributes to the interpretation of study results through all phases of clinical development. * Perform pharmacometric analyses to support drug ...
Senior Manager/Associate Director, Clinical Pharmacology
Princeton, NJ · On-site
$150K - $200K/yr
Perform quantitative pharmacology analyses and contributes to the interpretation of study results through all phases of clinical development. * Perform pharmacometric analyses to support drug ...
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Senior Manager/Associate Director, Clinical Pharmacology
Princeton, NJ · On-site
$150K - $200K/yr
Perform quantitative pharmacology analyses and contributes to the interpretation of study results through all phases of clinical development. * Perform pharmacometric analyses to support drug ...
Pharmacovigilance Expert - Remote
Atlanta, GA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
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Pharmacovigilance Expert - Remote
Atlanta, GA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
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Pharmacovigilance Expert - Remote
San Jose, CA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
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Pharmacovigilance Expert - Remote
San Jose, CA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
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Pharmacovigilance Expert - Remote
Chicago, IL · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
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Pharmacovigilance Expert - Remote
Chicago, IL · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
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Pharmacovigilance Expert - Remote
Seattle, WA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
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Pharmacovigilance Expert - Remote
Seattle, WA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Pharmacovigilance Expert - Remote
Phoenix, AZ · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
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Pharmacovigilance Expert - Remote
Phoenix, AZ · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
Quick apply
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
Pharmacovigilance Specialist
Los Angeles, CA · On-site
Title: Pharmacovigilance Specialist Location: Los Angeles, CA 90032 Duration- 4 months (Possible ... Responsible for data review, compilation, and analysis, including management of the integrated ...
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Pharmacovigilance Specialist
Los Angeles, CA · On-site
Title: Pharmacovigilance Specialist Location: Los Angeles, CA 90032 Duration- 4 months (Possible ... Responsible for data review, compilation, and analysis, including management of the integrated ...
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Quick apply
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
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Pharmacovigilance Expert - Remote
Boston, MA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
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Pharmacovigilance Expert - Remote
Boston, MA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
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Pharmacovigilance Expert - Remote
San Francisco, CA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Quick apply
Pharmacovigilance Expert - Remote
San Francisco, CA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
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Pharmacovigilance Expert - Remote
Washington, DC · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Quick apply
Pharmacovigilance Expert - Remote
Washington, DC · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Pharmacovigilance Expert - Remote
Boston, MA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Quick apply
Pharmacovigilance Expert - Remote
Boston, MA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Pharmacovigilance Expert - Remote
Philadelphia, PA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Quick apply
Pharmacovigilance Expert - Remote
Philadelphia, PA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Pharmacovigilance Expert - Remote
Houston, TX · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Quick apply
Pharmacovigilance Expert - Remote
Houston, TX · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Pharmacovigilance Expert - Remote
Seattle, WA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Quick apply
Pharmacovigilance Expert - Remote
Seattle, WA · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Pharmacovigilance Expert - Remote
Austin, TX · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Quick apply
Pharmacovigilance Expert - Remote
Austin, TX · Remote
$70 - $80/hr
Analyze aggregate safety data and reconcile case counts, figures, and inconsistencies across data sources. * Evaluate safety conclusions based on new data, events, and regulatory requirements.
New
Pharmacovigilance Analyst information
See salary details
$46K - $56.7K
8% of jobs
$56.7K - $67.5K
13% of jobs
$69.1K is the 25th percentile. Wages below this are outliers.
$67.5K - $78.2K
22% of jobs
The median wage is $85.2K / yr.
$78.2K - $88.9K
10% of jobs
$88.9K - $99.6K
4% of jobs
$99.6K - $110.4K
10% of jobs
$113.8K is the 75th percentile. Wages above this are outliers.
$110.4K - $121.1K
22% of jobs
$121.1K - $131.8K
5% of jobs
$131.8K - $142.5K
0% of jobs
$142.5K - $153.3K
1% of jobs
$153.3K - $164K
4% of jobs
$46K
$95.1K
$164K
How much do pharmacovigilance analyst jobs pay per year?
As of Aug 12, 2026, the average yearly pay for pharmacovigilance analyst in the United States is $95,100.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,000.00 and $118,000.00 per year, depending on experience, location, and employer.
What is the difference between Pharmacovigilance Analyst vs Pharmacovigilance Associate?
| Aspect | Pharmacovigilance Analyst | Pharmacovigilance Associate |
|---|---|---|
| Required Credentials | Bachelor's degree, training in drug safety, certifications like PV or RAC often preferred | Similar educational background, often entry-level with on-the-job training |
| Work Environment | Pharmaceutical companies, CROs, regulatory agencies; focus on data analysis and safety monitoring | Same settings; more administrative and data entry tasks |
| Employer & Industry Usage | Commonly employed in drug safety departments across pharma and biotech | Often an entry-level role within the same departments |
The main difference is that Pharmacovigilance Analysts typically handle data analysis and safety signal detection, while Pharmacovigilance Associates focus more on data entry and case processing. Both roles require similar qualifications and work in the same environments, but Analysts usually have more responsibility for interpreting safety data.
What are some common challenges faced by pharmacovigilance analysts when handling adverse event reports, and how are these addressed within the team?
Pharmacovigilance Analysts often face challenges such as incomplete or ambiguous information in adverse event reports, tight regulatory timelines, and the need to stay updated with evolving global regulations. To address these, teams typically implement thorough data verification processes, conduct regular training on regulations, and use collaborative tools for efficient case tracking. Analysts also work closely with medical reviewers, regulatory affairs, and other cross-functional teams to ensure accurate and timely reporting while maintaining compliance.
What does a pharmacovigilance analyst do?
A Pharmacovigilance Analyst is responsible for monitoring, assessing, and reporting on the safety and side effects of pharmaceutical products. They collect and analyze data on adverse drug reactions, ensure compliance with regulatory requirements, and help identify potential safety concerns. Their work is crucial in ensuring public health and drug safety by supporting risk management and regulatory decision-making throughout a product's life cycle.
What is the role of a pharmacovigilance analyst?
A pharmacovigilance analyst monitors and assesses the safety of pharmaceutical products by collecting, reviewing, and analyzing adverse drug reaction reports. They ensure compliance with regulatory requirements and use tools like safety databases to identify potential risks, supporting the overall drug safety process.
Is pharmacovigilance a good career path?
Pharmacovigilance is a growing field that involves monitoring the safety of pharmaceutical products, with roles like Pharmacovigilance Analyst requiring attention to detail, data analysis skills, and knowledge of regulatory guidelines. It offers opportunities in the pharmaceutical and healthcare industries, often with stable employment and potential for career advancement. Certification in pharmacovigilance and familiarity with safety databases can enhance job prospects.
What are the key skills and qualifications needed to thrive as a pharmacovigilance analyst, and why are they important?
To thrive as a Pharmacovigilance Analyst, you need a solid background in life sciences or pharmacy, strong analytical skills, and knowledge of drug safety regulations. Familiarity with pharmacovigilance databases (such as Argus or ARISg), MedDRA coding, and regulatory reporting systems is typically required, along with relevant certifications like GVP or ICH guidelines. Attention to detail, effective communication, and problem-solving abilities are essential soft skills in this role. These competencies ensure the accurate identification, assessment, and reporting of adverse drug events, which is critical for patient safety and regulatory compliance.
More about Pharmacovigilance Analyst jobs
What job categories do people searching Pharmacovigilance Analyst jobs look for? The top searched job categories for Pharmacovigilance Analyst jobs are:
Job description
Company Description
A Few Words About Us - Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
This position is with my direct clientÂ
Job Description
Serves as the Clinical Pharmacology representative and provides clinical pharmacology expertise on designated programs and clinical studies
Provides Clinical Pharmacology expertise for, but not limited to, the development of novel formulations (e.g. modified release)
Plans and directs clinical pharmacology components of clinical programs (including clinical development plan/life cycle plan) and studies (including synopsis preparation; clinical phase oversight, reporting)
Leads multifunctional study team to design, deliver and report the assigned clinical pharmacology studies and has overall scientific accountability for the designated studies.
Responsible for appropriate summarizing and interpreting results of pharmacokinetic/pharmacodynamics analyses with respect to their impact on development and clinical use of drugs.
Provides Clinical Pharmacology support for labelling requirements
Responsibilities-
Clinical Pharmacology representative on GEP programs / studies.
Responsible for providing the clinical pharmacology components of Clinical Plans and provides clinical pharmacology expertise to the project team.
Has an intimate understanding of the overall clinical development plan and works closely with the Clinical and Development Team to continually update and refine plan.
Assures that assigned CP study(ies) fulfils its role in the overall development plan
Plans, designs and oversees clinical pharmacology studies as required with operational assistance from Clinical Research Operations
Accountable and responsible for assigned synopsis and study report content
With study team, tracks emerging clinical pharmacology profile of the drug, keeps line management informed of changes in the profile as they occur in the assigned study(ies)
Must be fully knowledgeable about the clinical pharmacology profile of allocated drugs on which studies are being conducted or which are called for in the protocol.
Coordinates with medical writers (and other team members) in the data review, analysis and reporting of the CP study
Be responsible, in conjunction with medical writer, for overall content and accuracy of study report before forwarding for final sign-off
Assist with internal and external dissemination of results to Development Team, Investigators etc
Accountable and responsible for non-compartmental analysis of PK data and accountable for ensuring appropriate modelling and simulation in conjunction with Pharmacometrics.
Leads clinical pharmacology contributions to all regulatory documents including Investigator Brochures, Clinical Overviews, and regulatory filings.
Leads the resolution of clinical pharmacology queries from regulatory agencies, takes a lead role in writing and reviewing responses to regulatory queries
Qualifications
PhD or Pharm D -At least 10 years of general drug development experience in the pharmaceutical industry
At least 5 years' experience in clinical pharmacology work in the pharmaceutical industry
Demonstrated success in managing global clinical pharmacology activities
Experience in biopharmaceutic aspects of formulation development
Experience in interactions with regulatory agencies globally
Considerable organizational awareness (inter-relationship of departments, business priorities, etc.)
Additional Information
With Regards
Ricky Bansal
732-429-1925
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996