Global Pharmacovigilance Data Specialist

ProductLife Group; Florida; On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

International environment

Professional development

Job summary

ProductLife Group seeks a data professional to support pharmacovigilance and vigilance data management activities. You will ensure accurate processing, tracking, and maintenance of safety data while supporting regulatory compliance and operational excellence.

The role involves managing vigilance cases, database maintenance, reporting, and alignment with client and regulatory requirements within an international Life Sciences environment.

Qualifications

• Bachelor's degree in Life Sciences or related field.
• Experience in Pharmacovigilance, Drug Safety, or Regulatory Affairs is advantageous.
• Knowledge of pharmacovigilance regulations and safety databases preferred.

Responsibilities

• Manage vigilance cases and client mailboxes.
• Register and triage cases in tracking systems.
• Code medical information using MedDRA.
• Prepare case narratives and ensure data anonymization where needed.
• Support regulatory reporting to authorities.

Skills

Detail oriented

Proactive

Analytical mindset

Effective communication

Team oriented

Strong organizational skills

Critical thinking

Education

Bachelor's degree in Life Sciences

Tools

MedDRA coding

EudraVigilance

Microsoft Office

Job description

ProductLife Group seeks a data professional to support pharmacovigilance and vigilance data management activities. You will ensure accurate processing, tracking, and maintenance of safety data while supporting regulatory compliance and operational excellence.

The role involves managing vigilance cases, database maintenance, reporting, and alignment with client and regulatory requirements within an international Life Sciences environment.