... Preferred Qualifications: * RN, PharmD, or other healthcare certification * Experience with ... Pfizer, Amgen, Novartis, AbbVie, Merck Interview Process: * Round 1: Hiring Manager (Nancy Dubois)
... Preferred Qualifications: * RN, PharmD, or other healthcare certification * Experience with ... Pfizer, Amgen, Novartis, AbbVie, Merck Interview Process: * Round 1: Hiring Manager (Nancy Dubois)
Pfizer Rn information
What is a Pfizer RN?
What does a typical day look like for a Pfizer RN, and how does the role differ from traditional clinical nursing positions?
What are the key skills and qualifications needed to thrive as a Pfizer RN, and why are they important?
What is the difference between Pfizer Rn vs Pfizer Pharmacist?
| Aspect | Pfizer Rn | Pfizer Pharmacist |
|---|---|---|
| Required Credentials | Registered Nurse license, nursing degree | Pharmacy degree (Doctor of Pharmacy), licensure |
| Work Environment | Hospitals, clinics, healthcare settings | Pharmacies, healthcare facilities, research labs |
| Employer & Industry Usage | Healthcare providers, hospitals, clinics | Pharmaceutical 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.
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Other
Re-posted 5 days ago
Job description
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
- 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
- Maintain and update case tracking systems and databases
- Perform reconciliation with Medical Information, Quality, and external partners
- Develop and deliver training on adverse event reporting
- Support onboarding of new employees and vendors
- Assist in SOP creation and process documentation
- 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)
- 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
- Pharmacovigilance & Adverse Event Case Processing
- FDA / Health Canada Regulations
- ARGUS Safety Database
- Strong communication with patients & HCPs
- Critical thinking & escalation judgment
- 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
- CROs: IQVIA, Parexel, ICON, Syneos, PPD, Labcorp
- Pharma/Biotech: Pfizer, Amgen, Novartis, AbbVie, Merck
- Round 1: Hiring Manager (Nancy Dubois)
- Round 2: Senior Pharmacovigilance Team
- 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)