Groton, CT · On-site
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 ...
Groton, CT · On-site
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 ...
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 ...
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 ...
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 ...
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 ...
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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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 ...
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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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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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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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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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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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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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.
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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.
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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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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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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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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.
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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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.
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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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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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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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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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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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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.
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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.
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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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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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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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$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
| 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.
The top searched job categories for Pharmacovigilance Analyst jobs are:
Part-time
Re-posted 26 days ago
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 client
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
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.)
With Regards
Ricky Bansal
732-429-1925
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.
Recruiting and staffing services
51 - 200 Employees
Edison, NJ, US
1996
