Regulatory Affairs Professional

2 semanas atrás


Lisboa, Lisboa, Portugal Ergomed Tempo inteiro

**Overview**

We are Ergomed, a specialist pharmacovigilance service provider established in 2008.

We have achieved global organic growth year after year, with staff based across Europe, North America, and Asia.

We cover services within Medical Information, Pharmacovigilance, Regulatory Affairs, and Quality Assurance.

Our mission is to provide first-class support to our pharmaceutical and biotechnology partners.

Job Responsibilities

  • Manage various case processing services with full accountability
  • Work with teams of different sizes, from small clinical trials to large generic post-marketing teams
  • Process Individual Case Safety Reports from all sources (post-marketing and clinical trials, including device and combination products)
  • Perform and support contracted pharmacovigilance activities on behalf of PrimeVigilance

Requirements

Life science / biomedical background graduate or other healthcare-related degree qualification (chemistry, biology, biotechnology, veterinary science, etc.)

Demonstrated experience with several years in case processing

Benefits

An excellent training and development platform

A healthy work-life balance is critical for employee satisfaction



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