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Pharmacovigilance Analytics Jobs (NOW HIRING)

Pharmacovigilance Physician Venesco is seeking a Pharmacovigilance Physician to provide medical ... analyses, and regulatory safety reporting. Requirements: Duties and Responsibilities * Review and ...

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How much do pharmacovigilance analytics jobs pay per hour?

As of Jul 28, 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?

AspectPharmacovigilance AnalyticsPharmacovigilance Specialist
Required CredentialsDegree in life sciences, data analysis skills, certifications in pharmacovigilance or data analyticsDegree in pharmacy, life sciences, or healthcare; pharmacovigilance training or certification
Work EnvironmentData analysis teams, pharmacovigilance departments, often in pharmaceutical companies or CROsPharmacovigilance departments, clinical operations, regulatory teams
Employer & Industry UsageUsed in pharmaceutical companies, CROs, and analytics firms for data-driven safety monitoringUsed 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.

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:
Infographic showing various Pharmacovigilance Analytics job openings in the United States as of July 2026, with employment types broken down into 95% Full Time, 3% Part Time, and 2% Contract. Highlights an 80% Physical, 6% Hybrid, and 14% Remote job distribution, with an average salary of $96,145 per year, or $46.2 per hour.
Director, Clinical Pharmacology

Director, Clinical Pharmacology

Revolution Medicines

Redwood City, CA • Hybrid

Other

Posted 10 days ago


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. 

    #LI-Hybrid #LI-CT1