1

Pfizer Rn Jobs in Boston, MA (NOW HIRING)

Pfizer Rn information

What is a Pfizer RN?

A Pfizer RN is a registered nurse who works for Pfizer, a global pharmaceutical and biotechnology company. These nurses may be involved in clinical research, patient education, pharmacovigilance, or supporting the development and implementation of Pfizer’s healthcare products and therapies. Their roles often include collaborating with healthcare professionals, providing clinical expertise, and ensuring patient safety in clinical trials or product usage. Pfizer RNs play a key role in bridging the gap between medical research and patient care.

What does a typical day look like for a Pfizer RN, and how does the role differ from traditional clinical nursing positions?

As a Registered Nurse (RN) at Pfizer, your daily responsibilities often extend beyond direct patient care and may include supporting clinical trials, ensuring regulatory compliance, and collaborating with research teams. You might be involved in monitoring patient safety, educating participants, and maintaining detailed study documentation. The work environment is typically more structured and research-focused than a hospital setting, with frequent cross-functional collaboration with scientists, physicians, and regulatory specialists. This role offers RNs the opportunity to contribute to medical advancements while expanding their expertise in clinical research and pharmaceutical operations.

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

To excel as a Pfizer Registered Nurse, you need a solid background in clinical nursing, patient care, and a valid RN license, often complemented by experience in research or pharmaceutical settings. Familiarity with clinical trial protocols, electronic data capture (EDC) systems, and Good Clinical Practice (GCP) certification is highly valuable. Strong interpersonal communication, attention to detail, and adaptability are essential soft skills for collaborating with multidisciplinary teams and supporting trial participants. These competencies ensure patient safety, regulatory compliance, and the success of clinical research initiatives within the organization.

What is the difference between Pfizer Rn vs Pfizer Pharmacist?

AspectPfizer RnPfizer Pharmacist
Required CredentialsRegistered Nurse license, nursing degreePharmacy degree (Doctor of Pharmacy), licensure
Work EnvironmentHospitals, clinics, healthcare settingsPharmacies, healthcare facilities, research labs
Employer & Industry UsageHealthcare providers, hospitals, clinicsPharmaceutical companies, retail pharmacies, healthcare industry

Pfizer Rn and Pfizer Pharmacist roles both operate within the healthcare industry but focus on different areas. The Pfizer Rn provides patient care in clinical settings, requiring nursing credentials, while the Pfizer Pharmacist manages medication dispensing and counseling, requiring pharmacy licensure. Understanding these differences helps job seekers identify the right career path within Pfizer or similar organizations.

Does Pfizer pay well?

Pfizer RNs and other healthcare professionals are generally compensated with competitive salaries that reflect industry standards and experience levels. Pay can vary based on location, experience, and specific roles, often supplemented by benefits such as health insurance and retirement plans. Overall, Pfizer is considered to offer fair and competitive compensation for its employees in the pharmaceutical industry.

What are popular job titles related to Pfizer Rn jobs in Boston, MA?

For Pfizer Rn jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Pfizer Rn jobs in Boston, MA look for?

The top searched job categories for Pfizer Rn jobs in Boston, MA are:

Infographic showing various Pfizer Rn job openings in Boston, MA as of August 2026, with employment types broken down into 4% As Needed, 85% Full Time, and 11% Part Time. Highlights an 100% In-person job distribution.

Pharmacovigilance Specialist / Assistant

Kaav Inc.

Boston, MA • On-site

Other

Re-posted 5 days ago


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)