Pharmacovigilance Specialist: Global Safety & AE Reporting

Grifols, S.A

Los Angeles (CA)

On-site

USD 95,000 - 105,000

Full time

11 days ago
Application generator

An application made for this job — a tailored resume and cover letter that speak straight to the posting.

Get past ATS filters

Benefits offered by this job

Medical Insurance
Dental Insurance
Vision Insurance
Life Insurance
Paid Time Off
Paid holidays
401(k) match
Tuition Reimbursement

Job summary

Grifols, S.A. is seeking a Pharmacovigilance Specialist to provide operational support for global pharmacovigilance activities and ensure timely regulatory reporting. The role includes data review, analysis, and management of the integrated safety database.

Responsibilities include processing adverse event case reports, performing follow-up, notifying regulators, drafting PSURs, and contributing to SOPs and training. Travel within the United States may be required as part of CAPA and audits.

Qualifications

  • Bachelor’s degree in health sciences or bioscience; advanced degree preferred.
  • 1+ year of experience in pharmacovigilance, clinical research, or regulatory affairs in CRO/pharma.
  • 2–3 years in pharmacovigilance and adverse event reporting preferred.
  • Knowledge of EU and US pharmacovigilance practices and regulations.

Responsibilities

  • Manage adverse event case processing and follow-up.
  • Notify regulatory agencies and partners; respond to regulatory requests.
  • Draft and manage PSURs and signal detection reports; maintain filing/archiving.
  • Contribute to SOPs and training; support global pharmacovigilance operations.

Skills

Analytical skills
Communication skills
Autonomy

Education

Bachelor’s Degree in Health sciences
M.S. or Pharm.D. preferred

Tools

Safety databases

Job description

Grifols, S.A. is seeking a Pharmacovigilance Specialist to provide operational support for global pharmacovigilance activities and ensure timely regulatory reporting. The role includes data review, analysis, and management of the integrated safety database.

Responsibilities include processing adverse event case reports, performing follow-up, notifying regulators, drafting PSURs, and contributing to SOPs and training. Travel within the United States may be required as part of CAPA and audits.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Global Pharmacovigilance Specialist
Global Pharmacovigilance Specialist

Grifols • Los Angeles (CA)

On-site
USD 95,000 - 105,000
Medical insurance
Dental insurance
Vision insurance
+6
Pharmacovigilance Specialist
Pharmacovigilance Specialist

Grifols • Los Angeles (CA)

On-site
USD 95,000 - 105,000
Medical insurance
Dental insurance
Vision insurance
+6
Pharmacovigilance Specialist
Pharmacovigilance Specialist

Grifols, S.A • Los Angeles (CA)

On-site
USD 95,000 - 105,000
Medical Insurance
Dental Insurance
Vision Insurance
+5
Pharmacovigilance Data Analytics Manager — Global Safety
Pharmacovigilance Data Analytics Manager — Global Safety

Grifols, S.A • Clayton (NC)

On-site
USD 125,000 - 165,000
Manager, Pharmacovigilance Data Analysis
Manager, Pharmacovigilance Data Analysis

Grifols • North Carolina

On-site
USD 120,000 - 180,000
Manager, Pharmacovigilance Data Analysis 1
Manager, Pharmacovigilance Data Analysis 1

Grifols • North Carolina

On-site
USD 110,000 - 150,000
Global Pharmacovigilance Data & Systems Lead
Global Pharmacovigilance Data & Systems Lead

Grifols • North Carolina

On-site
USD 120,000 - 180,000
Manager, Pharmacovigilance Data Analysis
Manager, Pharmacovigilance Data Analysis

Grifols, S.A • Clayton (NC)

On-site
USD 120,000 - 160,000
Lead Pharmacovigilance Data Analytics
Lead Pharmacovigilance Data Analytics

Grifols, S.A • Clayton (NC)

On-site
USD 120,000 - 160,000
Manager, Pharmacovigilance Data Analysis 1
Manager, Pharmacovigilance Data Analysis 1

Grifols, S.A • Clayton (NC)

On-site
USD 125,000 - 165,000