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Specialist Clinical Safety

Cencora

Madrid

A distancia

EUR 30.000 - 45.000

Jornada completa

Hoy
Sé de los primeros/as/es en solicitar esta vacante

Descripción de la vacante

A global health organization is seeking a motivated PV Specialist for their Clinical Safety team in Spain. Key responsibilities include managing safety event reports, supporting the Safety Manager, and maintaining safety databases. Candidates should possess a Bachelor’s degree in a relevant field and at least 1 year of experience in Pharmacovigilance. Fluency in English and strong organizational skills are essential. Join a dedicated team focused on improving health outcomes!

Formación

  • 1+ years of relevant experience in Pharmacovigilance.
  • Knowledge of safety databases essential.
  • Experience in case management activities.

Responsabilidades

  • Manage SAEs / AESIs and ensure all parties are informed.
  • Initial triage for SAEs and data entry in safety database.
  • Support Safety Manager with case reviews and maintain trackers.

Conocimientos

Team-oriented approach
Organizational skills
Self-motivation
Flexibility and adaptability
Fluent English
Excellent communication skills

Educación

Bachelor’s in medical or natural sciences
Degree in Medicine

Herramientas

Argus
Safety Easy
Descripción del empleo
Overview

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!

Job Details

PV specialist – Clinical Safety

We have an exciting opportunity for a PV Specialist to join our Clinical Safety team! This role can be based remotely in Spain and we are, above all else, looking for an individual who is motivated and enthusiastic to grow with our Pharmalex brand which has seen great success.

Responsibilities
  • Management of SAEs / AESIs / pregnancies
  • Assure all parties are informed as required & querying the sites when needed; follow the whole process for each case / remind parties of pending information when applicable.
  • Initial triage (assessment of expectedness / seriousness) of SAEs.
  • Data Entry in safety database
  • Narrative writing
  • Support Safety Manager with Review of cases in safety database (QC)
  • Preparation of Line Listings
  • Maintaining annual plans for LLs / DSURs and distribution lists.
  • Safety submissions.
  • Maintenance of trackers and other administrative activities.
Skills
  • Team-oriented approach
  • Organizational skills, ability to multi-task. Ability to assimilate and analyse information rapidly.
  • High sense of responsibility and self-motivation
  • Highly service-oriented
  • Flexibility and adaptability to adjust rapidly to new, unknown, challenging situations.
  • Fluent written and spoken English skills.
  • Excellent written and verbal communication skills.
Experience / Background
  • Successful completion of a Bachelor’s degree in medical, natural sciences or pharmacy-related field or Degree in Medicine
  • At least 1 year of relevant professional experience in the field of Pharmacovigilance.
  • Knowledge of safety databases (Argus, Safety Easy are preferred)
  • Experience in case management activities
  • Previous experience in pre-authorisation area.
What Cencora offers

Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.

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