LATAM Pharmacovigilance & Safety Analyst

IQVIA LLC; Santiago; Hybrid; CLP 13,392,000 - 31,248,000; Full time

Job summary

IQVIA LLC is seeking a Pharmacovigilance Analyst located in Santiago, Chile, to support LATAM safety activities across client projects. Responsibilities include adverse event identification, data source review, client reporting, and regulatory compliance support.

You will contribute to safety deliverables, QA checks, audits, and process improvements while collaborating with PMR, CES, Consulting, Quality, and Operations teams.

Qualifications

• Bachelor’s degree in life sciences or related field required.
• 2–4 years of pharmacovigilance or lifecycle safety experience.
• Knowledge of AE reporting, timelines, and LATAM regulatory expectations.

Responsibilities

• Identify and review adverse events and safety information.
• Ensure timely AE reporting per contractual timelines and local requirements.
• Develop and maintain PV documentation, trackers, and reporting specs.
• Collaborate with cross-functional teams to ensure safety oversight.
• Support audits, CAPA activities, and process improvement initiatives.

Skills

Adverse event identification

Safety reporting timelines

Data source review

Client reporting

Quality checks

CAPA

Regulatory compliance

Analytical thinking

Communication

Education

Bachelor’s degree in Life Sciences or related field

Tools

Pharmacovigilance systems

Regulatory guidelines (GVP)

Audit preparation tools

Job description

IQVIA LLC is seeking a Pharmacovigilance Analyst located in Santiago, Chile, to support LATAM safety activities across client projects. Responsibilities include adverse event identification, data source review, client reporting, and regulatory compliance support.

You will contribute to safety deliverables, QA checks, audits, and process improvements while collaborating with PMR, CES, Consulting, Quality, and Operations teams.