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How much do pfizer pharmd jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for pfizer pharmd in the United States is $22.63, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $25.00 per hour, depending on experience, location, and employer.

What does a Pfizer PharmD do?

A Pfizer PharmD is a Doctor of Pharmacy who works at Pfizer, typically playing a key role in drug development, clinical trials, regulatory affairs, or medical affairs. Their responsibilities may include evaluating clinical data, ensuring medication safety, providing scientific expertise, and supporting educational initiatives for healthcare professionals. They collaborate with cross-functional teams to ensure the safe and effective use of Pfizer's pharmaceutical products. This role often requires strong clinical knowledge, communication skills, and a commitment to advancing public health.

What are typical responsibilities and collaborative opportunities for a Pfizer PharmD?

As a PharmD at Pfizer, your daily responsibilities may include reviewing clinical trial data, contributing to drug safety assessments, and providing scientific expertise to cross-functional teams. You’ll often collaborate with colleagues in clinical development, regulatory affairs, and medical affairs to support the advancement of new therapies. This role offers the chance to work in a highly collaborative, fast-paced environment, and you’ll frequently engage in multidisciplinary projects that can broaden your professional experience and open up opportunities for career progression within the company.

What are the key skills and qualifications needed to thrive as a Pfizer PharmD, and why are they important?

To thrive as a Pfizer PharmD, you need an advanced pharmacy degree (PharmD), strong clinical knowledge, and expertise in pharmacology and drug development. Familiarity with regulatory requirements, medical information systems, and tools like MedDRA or clinical trial databases is typically required. Exceptional communication, analytical thinking, and teamwork skills help you effectively collaborate across multidisciplinary teams and convey complex information. These competencies are crucial to ensure safe, effective medication use and to support Pfizer’s research, development, and regulatory objectives.

What is the difference between Pfizer Pharmd vs CVS Pharmacist?

AspectPfizer PharmdCVS Pharmacist
Required CredentialsDoctor of Pharmacy (PharmD), state licensureDoctor of Pharmacy (PharmD), state licensure
Work EnvironmentResearch, development, or corporate settings within PfizerRetail pharmacy, community setting
Employer & IndustryPharmaceutical industry, healthcare, researchRetail pharmacy chain, healthcare services

The Pfizer Pharmd typically works in research, development, or corporate roles within Pfizer, focusing on drug development and healthcare solutions. In contrast, a CVS Pharmacist works directly with patients in retail pharmacy settings, dispensing medications and providing healthcare advice. Both roles require a PharmD degree and licensure but differ significantly in work environment and daily responsibilities.

Does Pfizer Pharmd pay well?

Pfizer PharmD professionals typically earn competitive salaries that reflect their advanced clinical training and expertise. Compensation can vary based on experience, location, and specific roles within the company, with many positions offering additional benefits such as bonuses and health insurance.
More about Pfizer Pharmd jobs

What states have the most Pfizer Pharmd jobs?

States with the most job openings for Pfizer Pharmd jobs include:

What job categories do people searching Pfizer Pharmd jobs look for?

The top searched job categories for Pfizer Pharmd jobs are:

Pfizer Pharmd jobs near you
Infographic showing various Pfizer Pharmd job openings in the United States as of August 2026, with employment types broken down into 2% As Needed, 82% Full Time, 15% Part Time, and 1% Contract. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $47,067 per year, or $22.6 per hour.

Pharmacovigilance Specialist / Assistant

Kaav Inc.

Boston, MA • On-site

Other

This job post has expired 2 days ago. Applications are no longer accepted.

Job description

Job Title: Pharmacovigilance Specialist / Assistant
Location: Remote (Candidates in Fort Worth, TX or Boston, MA preferred for future hybrid)
Job Summary:
seeking a Pharmacovigilance Specialist to support adverse event case processing and safety reporting. This role is highly interactive and requires working closely with patients, healthcare professionals (HCPs), vendors, and internal teams.
The ideal candidate will have strong experience in drug safety, case processing, and regulatory compliance (FDA/Health Canada), along with the ability to operate in a fast-paced, high-volume environment.
Key Responsibilities:
Adverse Event Case Management (50%)
  • Review and evaluate incoming communications (phone, email, fax, etc.) for adverse event (AE) reporting
  • Perform medical evaluation of AE cases for seriousness and reporting requirements
  • Process and manage cases in safety databases (e.g., ARGUS)
  • Conduct follow-ups to gather missing or additional case information
  • Prepare and submit expedited and periodic safety reports to FDA and Health Canada
  • Ensure AE intake from marketing programs and social media platforms
  • Support audits and regulatory inspections
  • Perform trend analysis and signal detection reporting
Regulatory & Product Knowledge (25%)
  • Maintain knowledge of FDA & Health Canada pharmacovigilance regulations
  • Understand company SOPs, drug safety processes, and compliance requirements
  • Develop knowledge of Galderma products and dermatology-related conditions
Data & Case Tracking (15%)
  • Maintain and update case tracking systems and databases
  • Perform reconciliation with Medical Information, Quality, and external partners
Training & Support (10%)
  • Develop and deliver training on adverse event reporting
  • Support onboarding of new employees and vendors
  • Assist in SOP creation and process documentation
Required Qualifications:
  • Bachelor's degree in Life Sciences, Healthcare, or related field
  • 5+ years of Pharmacovigilance / Drug Safety experience
  • Strong experience in case processing and adverse event reporting
  • Knowledge of FDA and Health Canada safety regulations
  • Hands-on experience with ARGUS or similar safety databases
  • Strong understanding of medical terminology and drug safety concepts
  • Ability to handle patient and HCP interactions (including sensitive discussions)
Preferred Qualifications:
  • RN, PharmD, or other healthcare certification
  • Experience with biologics, drugs, or combination products
  • Background in CROs or Pharma/Biotech companies
  • Experience in SOP writing and training delivery
  • Exposure to global pharmacovigilance environments
Top Skills Required:
  • Pharmacovigilance & Adverse Event Case Processing
  • FDA / Health Canada Regulations
  • ARGUS Safety Database
  • Strong communication with patients & HCPs
  • Critical thinking & escalation judgment
Soft Skills:
  • Self-driven and able to work independently in remote setup
  • Strong communication and collaboration skills
  • Ability to handle high-volume workload and prioritize effectively
  • Comfortable in externally facing, high-visibility role
Nice-to-Have Background:
  • CROs: IQVIA, Parexel, ICON, Syneos, PPD, Labcorp
  • Pharma/Biotech: Pfizer, Amgen, Novartis, AbbVie, Merck
Interview Process:
  • Round 1: Hiring Manager (Nancy Dubois)
  • Round 2: Senior Pharmacovigilance Team
Additional Notes:
  • Immediate need due to high case volume and understaffing
  • Role is highly visible and interactive, not just backend processing
  • Potential for future conversion (must be open to hybrid in TX or MA)

Apply