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 ...
Sr. 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 ...
Quick apply
Sr. 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 ...
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.
Quick apply
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.
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.
Quick apply
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.
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.
Quick apply
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.
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.
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.
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.
Quick apply
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.
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.
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 Expert - Remote
Dallas, 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.
Quick apply
Pharmacovigilance Expert - Remote
Dallas, 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.
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.
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.
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.
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.
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 ...
Quick apply
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 ...
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.
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.
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.
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.
Pharmacovigilance Expert - Remote
Los Angeles, 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.
Quick apply
Pharmacovigilance Expert - Remote
Los Angeles, 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.
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.
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.
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.
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.
Pharmacovigilance Analytics information
See salary details
$27.89 is the 25th percentile. Wages below this are outliers.
$22.84 - $28.37
27% of jobs
$28.37 - $33.89
3% of jobs
$33.89 - $39.42
11% of jobs
The median wage is $42.36 / hr.
$39.42 - $44.95
17% of jobs
$44.95 - $50.48
11% of jobs
$52.78 is the 75th percentile. Wages above this are outliers.
$50.48 - $56.01
16% of jobs
$56.01 - $61.54
8% of jobs
$61.54 - $67.07
4% of jobs
$67.07 - $72.60
0% of jobs
$72.60 - $78.13
0% of jobs
$78.13 - $83.65
3% of jobs
$22
$46
$83
How much do pharmacovigilance analytics jobs pay per hour?
As of Aug 19, 2026, the average hourly pay for pharmacovigilance analytics in the United States is $46.22, according to ZipRecruiter salary data. Most workers in this role earn between $26.92 and $55.29 per hour, depending on experience, location, and employer.
What is the difference between Pharmacovigilance Analytics vs Pharmacovigilance Specialist?
| Aspect | Pharmacovigilance Analytics | Pharmacovigilance Specialist |
|---|---|---|
| Required Credentials | Degree in life sciences, data analysis skills, certifications in pharmacovigilance or data analytics | Degree in pharmacy, life sciences, or healthcare; pharmacovigilance training or certification |
| Work Environment | Data analysis teams, pharmacovigilance departments, often in pharmaceutical companies or CROs | Pharmacovigilance departments, clinical operations, regulatory teams |
| Employer & Industry Usage | Used in pharmaceutical companies, CROs, and analytics firms for data-driven safety monitoring | Used in pharma companies, hospitals, and regulatory agencies for safety reporting and compliance |
Pharmacovigilance Analytics focuses on analyzing safety data, utilizing data science and statistical tools, while Pharmacovigilance Specialists handle case processing, safety reporting, and compliance. Both roles are essential in drug safety but differ in their core functions and skill sets.
What does a pharmacovigilance analyst do?
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, often using specialized databases and tools, and contribute to risk management and safety reporting processes within pharmaceutical or healthcare organizations.
What is pharmacovigilance analytics?
Pharmacovigilance analytics involves analyzing data related to drug safety and adverse events to identify potential risks associated with medications. Professionals in this field use statistical tools and databases to monitor, assess, and report safety signals, supporting regulatory compliance and patient safety efforts.
More about Pharmacovigilance Analytics jobs
What cities are hiring for Pharmacovigilance Analytics jobs?
Cities with the most Pharmacovigilance Analytics job openings:
What states have the most Pharmacovigilance Analytics jobs?
States with the most job openings for Pharmacovigilance Analytics jobs include:
What job categories do people searching Pharmacovigilance Analytics jobs look for?
The top searched job categories for Pharmacovigilance Analytics 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