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Company Description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Start up Specialist office based in Denmark.

Job Overview
  • Responsible for CA & Ethics Committee (EC) submission
  • Keep up to date knowledge of GCP and ICH Guidelines for clinical research.
  • Translation and co-ordination of translations for documents required for submissions.
  • Supervising study conduct according to GCP requirements and all applicable laws.
Key Requirements
  • Bachelor degree in life-science
  • Min 2 years in EC & CA submissions within a CRO, Pharma, Biotech¬† in Denmark
  • Experience in clinical studies phase II-III
  • Excellent communication skills
  • Fluent Swedish & Norwegian
  • FTE: 1.0

 

Tagged as: start up jobs

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