LATAM Pharmacovigilance Analyst: Safety Data & Reporting

IQVIA Argentina

Santiago

In loco

CLP 15.000.000 - 35.000.000

Tempo pieno

2 giorni fa
Candidati tra i primi
Generatore di candidature

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Descrizione del lavoro

IQVIA is a leading global provider of clinical research services and healthcare insights, seeking a Pharmacovigilance Analyst to support LATAM projects. You will review data sources, identify adverse events, and ensure timely reporting to clients in line with contracts and local requirements.

The role involves collaborating with cross‑functional teams, maintaining PV documentation, and contributing to process improvements, audits, and client safety deliverables while staying current with LATAM

Competenze

  • Bachelor's degree in life sciences or related field is required.
  • 2–4 years of related PV, lifecycle safety, clinical safety, quality, regulatory, or life sciences ops experience.
  • Strong understanding of adverse event identification, safety reporting timelines and PV concepts.
  • Knowledge of PV regulations, GVP principles, and LATAM safety requirements preferred.
  • Ability to review scientific, medical, and operational documentation with accuracy.
  • Strong analytical, organizational, and time management skills.
  • Effective communication and collaboration with internal teams and clients.
  • Experience supporting audits, quality checks, CAPA, reconciliations or process improvements is desirable.

Mansioni

  • Reviews project materials and data to identify potential safety signals.
  • Ensures timely adverse event reporting to clients per timelines and local requirements.
  • Supports PV documentation, trackers, procedures, training materials and reporting specs.
  • Performs qualitative reviews of safety information for accuracy and compliance.
  • Supports client deliverables including AE reports, reconciliations, audit responses, metrics.
  • Collaborates with cross-functional teams for safety oversight across projects.
  • Supports quality management activities, including QC checks and CAPA support.
  • Contributes to RFP reviews, project start-up activities, and client discussions with PV input.
  • Keeps up-to-date with LATAM regulations and GVP principles.
  • May train junior analysts on AE identification and reporting requirements.

Conoscenze

Analytical skills
Organizational skills
Time management
Communication skills
Attention to detail

Formazione

Bachelor’s Degree in Life Sciences, Pharmacy, Nursing, Medicine, Biology, Chemistry, or related health/scientific field

Descrizione del lavoro

IQVIA is a leading global provider of clinical research services and healthcare insights, seeking a Pharmacovigilance Analyst to support LATAM projects. You will review data sources, identify adverse events, and ensure timely reporting to clients in line with contracts and local requirements.

The role involves collaborating with cross‑functional teams, maintaining PV documentation, and contributing to process improvements, audits, and client safety deliverables while staying current with LATAM

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