Apply state-of-the-art quantitative pharmacology analyses, including population PK, exposure-response analyses, to guide dose/schedule selection and recommended phase 2 dose and schedule (RP2Ds ...
Apply state-of-the-art quantitative pharmacology analyses, including population PK, exposure-response analyses, to guide dose/schedule selection and recommended phase 2 dose and schedule (RP2Ds ...
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 ...
Director, Anti-infective Pharmacology
$210K - $250K/yr
Data Analysis and Interpretation: o Analyze and interpret preclinical and clinical pharmacology data to guide decision-making and optimize compound selection and progression. o Generate high-quality ...
Director, Anti-infective Pharmacology
$210K - $250K/yr
Data Analysis and Interpretation: o Analyze and interpret preclinical and clinical pharmacology data to guide decision-making and optimize compound selection and progression. o Generate high-quality ...
Director, Anti-infective Pharmacology
San Diego, CA · On-site
$210K - $250K/yr
Data Analysis and Interpretation: o Analyze and interpret preclinical and clinical pharmacology data to guide decision-making and optimize compound selection and progression. o Generate high-quality ...
Director, Anti-infective Pharmacology
San Diego, CA · On-site
$210K - $250K/yr
Data Analysis and Interpretation: o Analyze and interpret preclinical and clinical pharmacology data to guide decision-making and optimize compound selection and progression. o Generate high-quality ...
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 ...
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 ...
It oversees the preparation and authorization of PK analysis reports, CSR content, and clinical pharmacology components of global regulatory submissions Responsibilities * Provide Clinical ...
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It oversees the preparation and authorization of PK analysis reports, CSR content, and clinical pharmacology components of global regulatory submissions Responsibilities * Provide Clinical ...
Senior Scientist / Principal Scientist, Clinical Pharmacology
Madison, WI · On-site
$120K - $170K/yr
It oversees the preparation and authorization of PK analysis reports, CSR content, and clinical pharmacology components of global regulatory submissions Responsibilities * Provide Clinical ...
Senior Scientist / Principal Scientist, Clinical Pharmacology
Madison, WI · On-site
$120K - $170K/yr
It oversees the preparation and authorization of PK analysis reports, CSR content, and clinical pharmacology components of global regulatory submissions Responsibilities * Provide Clinical ...
... Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients ... The Pharmacovigilance Scientist (PVS) will serve as a core member of the safety team and is ...
... Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients ... The Pharmacovigilance Scientist (PVS) will serve as a core member of the safety team and is ...
Collaborate cross functionally to access and utilize data visualization and analysis tools for ... Provide content for pharmacovigilance training as needed * Contribute to the implementation of ...
Collaborate cross functionally to access and utilize data visualization and analysis tools for ... Provide content for pharmacovigilance training as needed * Contribute to the implementation of ...
Pharmacovigilance Physician
Frederick, MD · On-site
Pharmacovigilance Physician Venesco is seeking a Pharmacovigilance Physician to provide medical ... analyses, and regulatory safety reporting. Requirements: Duties and Responsibilities * Review and ...
New
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Pharmacovigilance Physician
Frederick, MD · On-site
Pharmacovigilance Physician Venesco is seeking a Pharmacovigilance Physician to provide medical ... analyses, and regulatory safety reporting. Requirements: Duties and Responsibilities * Review and ...
New
Oversees Clinical Pharmacology deliverables, including analysis plans, reports, and contributions to regulatory documents (e.g., INDs, CTAs, NDAs, briefing books, Investigator Brochures) * Applies ...
Oversees Clinical Pharmacology deliverables, including analysis plans, reports, and contributions to regulatory documents (e.g., INDs, CTAs, NDAs, briefing books, Investigator Brochures) * Applies ...
Oversees Clinical Pharmacology deliverables, including analysis plans, reports, and contributions to regulatory documents (e.g., INDs, CTAs, NDAs, briefing books, Investigator Brochures) * Applies ...
Oversees Clinical Pharmacology deliverables, including analysis plans, reports, and contributions to regulatory documents (e.g., INDs, CTAs, NDAs, briefing books, Investigator Brochures) * Applies ...
Principal Investigator / Sr. Principal Investigator, Clinical Pharmacology & Pharmacometrics
Wilmington, DE · On-site
Provide guidance in interpreting the data from quantitative pharmacology analyses, including PPK, exposure-response analyses, and other quantitative analyses, to drive MIDD based decision making for ...
Principal Investigator / Sr. Principal Investigator, Clinical Pharmacology & Pharmacometrics
Wilmington, DE · On-site
Provide guidance in interpreting the data from quantitative pharmacology analyses, including PPK, exposure-response analyses, and other quantitative analyses, to drive MIDD based decision making for ...
The Director of Pharmacovigilance (PV) will play a critical role in executing Umoja Biopharma ... Support signal detection activities, including data review, trend analysis, and documentation
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The Director of Pharmacovigilance (PV) will play a critical role in executing Umoja Biopharma ... Support signal detection activities, including data review, trend analysis, and documentation
Director, Pharmacovigilance
Philadelphia, PA · On-site +1
This role is responsible for ensuring high-quality safety data collection, analysis, and reporting ... Lead pharmacovigilance strategy across clinical programs, ensuring alignment with overall clinical ...
Director, Pharmacovigilance
Philadelphia, PA · On-site +1
This role is responsible for ensuring high-quality safety data collection, analysis, and reporting ... Lead pharmacovigilance strategy across clinical programs, ensuring alignment with overall clinical ...
Director, Pharmacovigilance
Philadelphia, PA · On-site +1
This role is responsible for ensuring high-quality safety data collection, analysis, and reporting ... Lead pharmacovigilance strategy across clinical programs, ensuring alignment with overall clinical ...
Director, Pharmacovigilance
Philadelphia, PA · On-site +1
This role is responsible for ensuring high-quality safety data collection, analysis, and reporting ... Lead pharmacovigilance strategy across clinical programs, ensuring alignment with overall clinical ...
Director, Clinical Pharmacology
Redwood City, CA · On-site
$211K - $264K/yr
Apply state-of-the-art quantitative pharmacology analyses, including population PK, exposure-response analyses, to guide dose/schedule selection and recommended phase 2 dose and schedule (RP2Ds ...
Director, Clinical Pharmacology
Redwood City, CA · On-site
$211K - $264K/yr
Apply state-of-the-art quantitative pharmacology analyses, including population PK, exposure-response analyses, to guide dose/schedule selection and recommended phase 2 dose and schedule (RP2Ds ...
Perform safety data analyses, draft query responses, and prepare documents for cross functional ... Familiarity with pharmacovigilance and drug development, including knowledge of applicable clinical ...
Perform safety data analyses, draft query responses, and prepare documents for cross functional ... Familiarity with pharmacovigilance and drug development, including knowledge of applicable clinical ...
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?
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.

Job description
The Opportunity:
We are seeking a highly motivated and energetic individual with a relevant scientific background to be part of the Nonclinical Development and Clinical Pharmacology (NDCP) Organization.
As a key member of the Clinical Pharmacology group, you will:
Represent the clinical pharmacology function in project teams and build strong working relationships with cross-functional teams to impact critical decisions.
Responsible for clinical pipeline delivery through major milestones including IND/CTA, EOP2, and marketing applications NDA/sNDA.
Lead the design and execution of an integrated clinical pharmacology and modeling and simulation strategy to guide the clinical development plan.
Apply state-of-the-art quantitative pharmacology analyses, including population PK, exposure-response analyses, to guide dose/schedule selection and recommended phase 2 dose and schedule (RP2Ds) selection.
Author and provide technical input for regulatory documents and submissions related to all aspects of clinical pharmacology (including protocol, CSR, IB, briefing package, SCP/SBS, label etc) and responses to regulatory questions.
Engage and work with consultants and/or CROs on clinical pharmacology activities to complement in-house knowledge/expertise and capacities.
Ability to manage internship and fellowship programs.
Required Experience, Skills, and Education:
A Ph.D. or Pharm.D or equivalence with 7+ years of relevant industry experience in Clinical and Quantitative pharmacology.
Expertise in clinical pharmacology, hands-on modeling, and simulation skills using NONMEM, R, and/or other modeling and simulation software. Experience with population PK, exposure-response, and advanced mechanistic PK/PD models.
Track record of applying modeling and simulation methodologies to inform and accelerate drug development.
Well-informed in current and emerging scientific standards of regulatory requirements and expectations.
Excellent verbal and written communication skills, and ability to clearly convey complex concepts and findings to both non-specialist and specialist audiences.
Strong interpersonal skills, and ability to influence development project and management teams.
A critical thinker and passionate team player with high energy who thrives in a dynamic and fast-paced environment.
Preferred Skills:
Prior experience with small molecules in oncology drug development.
Proven successful industry experience in oncology submissions in the US, EU and Asia.
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