Junior Pharmacovigilance Associate

United Consulting Hub, Inc.; United States; Remote; USD 34,000 - 55,000; Full time

Job summary

United Consulting Hub, Inc. seeks a motivated Junior Pharmacovigilance Associate to support drug safety monitoring in pharma/biotech. The role focuses on processing adverse event reports, safety documentation, and regulatory compliance in a remote, contract setting.

Ideal candidates have 0–2 years' experience, strong written communication, and attention to detail. You will collaborate with safety teams, maintain databases, and assist with ICSRs and periodic safety reports.

Qualifications

• Basic understanding of pharmacology and drug safety.
• Familiarity with adverse event reporting and safety documentation.
• Strong analytical and documentation skills.
• Good written communication and attention to detail.

Responsibilities

• Assist in collecting and processing adverse event reports.
• Support the preparation of ICSRs.
• Review safety information for completeness and accuracy.
• Maintain pharmacovigilance databases and safety records.
• Assist with literature screening for drug safety information.
• Support the preparation of periodic safety reports.
• Track case processing timelines and regulatory reporting requirements.
• Follow company SOPs and applicable pharmacovigilance guidelines.

Skills

Pharmacovigilance basics

Adverse event reporting

Analytical documentation

Attention to detail

Job description

Job Title: Junior Pharmacovigilance Associate

Type: Contract

Location: Remote

Experience: 0-2 years

Job Summary:

We are seeking a motivated Junior Pharmacovigilance Associate to support drug safety monitoring activities in the pharmaceutical and biotechnology industries. The candidate will assist in processing adverse event reports, maintaining safety documentation, and supporting compliance with pharmacovigilance regulations.

Key Responsibilities:

• Assist in collecting and processing adverse event reports.
• Support the preparation of Individual Case Safety Reports (ICSRs).
• Review safety information for completeness and accuracy.
• Maintain pharmacovigilance databases and safety records.
• Assist with literature screening for drug safety information.
• Support the preparation of periodic safety reports.
• Track case processing timelines and regulatory reporting requirements.
• Follow company SOPs and applicable pharmacovigilance guidelines.

Skills Required:

• Basic understanding of pharmacology and drug safety.
• Familiarity with adverse event reporting and safety documentation.
• Strong analytical and documentation skills.
• Good written communication and attention to detail.

Preferred:

• Internship or academic project experience in pharmacovigilance.
• Familiarity with safety databases and ICH guidelines.