Pharmacovigilance Analyst

Colombia Temporal COP4,000,000 - COP4,400,000 por mes (COP48,000,000 - COP52,800,000 por año) Descripción de Vacante
The Pharmacovigilance Analyst position requires experience in monitoring, recording, and analyzing data related to drug safety. This role is key in the life sciences sector and is based in Bogotá D.C.

Fecha de publicación 09/02/2026

  • You will have the opportunity to grow professionally
  • You will join a role that allows you to develop new skills

Acerca de nuestro cliente

The purpose of the role is to ensure affiliate compliance with internal and external requirements concerning Pharmacovigilance (PhV) in aligned countries. In the absence of the primary PhV role, the PhV backup shall take up key responsibilities

Descripción

* Execute pharmacovigilance activities as nationally required (such as adverse event management, expedited and periodic reporting).

* Responsible for appropriate communication between local product safety, Global Patient Safety (GPS), and other relevant stakeholders (product complaints, medical affairs, and regulatory affairs).

* Provide local training (initial and/or refresher) for employees and/or business alliance partners to raise awareness of PhV, as required.

* Strive for inspection and audit readiness, and participate in aligned affiliate inspections, audits, and assessments.

* Help interpret relevant regulations and guidelines and act as a contact person within the affiliate.

* Responsible for ensuring compliance with Ministry of Health/Regulatory Authority (MoH/RA) requirements and GPS policies, procedures, and processes.

Serve as the point of contact for the receipt and collection of AE reports.

* Enter adverse event/device cases into the safety database.

* Ensure that all relevant information is captured and forwarded to GPS within the designated timeframe, for both initial and follow-up reports.

* Be responsible for the accuracy and completeness of information reported from clinical trials, post‑marketing studies, and spontaneous adverse events for marketed products and devices.

* Complete case follow‑up as directed or required.

* Be responsible for generating and submitting the necessary case reports required for expedited reporting to the MoH/RA.

* Reconcile case reports with business partners, medical information, and product quality.

* Archive case source documentation.

Perfil buscado (h/m)

Bachelor's degree in a health profession (such as Pharmacy or Nursing) or a life science field, or equivalent demonstrated experience in patient safety.

Knowledge and understanding of applicable local, regional, and global procedures.

Knowledge of legislation regarding national regulatory guidelines, directives, and regulations in Pharmacovigilance.

Qué Ofrecemos

An organized work environment focused on professional excellence.

The opportunity to work in Bogotá D.C., a strategic location for the healthcare industry.

Ongoing training in pharmacovigilance regulations and processes.

Corporate benefits that support well-being and personal development.

A monthly salary of 4,000,000.

The position requires a B2 level of English.

Contacto
Estefany Cely
Ingresar referencia para vacante
JN-022026-6943638

Resumen de empleo

Sector
Healthcare & Life Sciences
Sub Sector
Registros
Sector
Healthcare / Pharmaceutical
Ubicación
Colombia
Tipo de Trabajo
Temporal
Nombre del consultor
Estefany Cely
Job Reference
JN-022026-6943638

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