Consultant – Safety Data Analytics (m/f) – Freelance – geschlossen

  • Position zu besetzen ab 13. August 2018
  • Permanent-ID OCR-FL-2018-1132
  • Branche Pharma
  • Beschäftigungsform Freelance/ Contracting
  • Standort Deutschland / 6x
  • Kategorien Beschäftigungsform, Branche, Freelance/Contracting, Pharma

Aufgaben

As a Consultant of post-marketing Safety Data Analytics you will be working in a small team of PV Data experts (3) to build up a framework, and design appropriate diagrams & visualizations to summarize and communicate the safety data in a transparent way.

These tools will support the Safety Physicians, scientists and Medical team in the R&D organisation to conduct a meaningful medical assessment of safety data in the context of Benefit/risk. Furthermore to support all parties when addressing Ad-Hoc queries from external stakeholders including HA.

Anforderungen

  • Experience in the Pharmaceutical Industry and /or CROs > 5 yrs.
  • Pharmacoepidemiology Analytic – Clinical&Safety data analysis > 5 yrs.
  • Experience in Diagram/ Visualizations to summarize & communicate the data in a transparent way > 5 yrs.
  • Understanding of Observational data/Clinical Trials and translation of the data > 5 yrs.
  • Scientific Degree in Pharmaco-epidemiology and/ or Statistics would be an asset
  • Expertise in the field of Global drug safety would be an asset

Zusätzliche Informationen

Standort: Darmstadt

Projektbeginn: August/September 2018

Projektlaufzeit: 120 Tage bis 31.01.2019

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