Start up Specialist Denmark
Full Time
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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
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