WHAT AWAITS YOU:

• You will be responsible for planning, conducting, analyzing and interpreting clinical studies and trials with the aim of ensuring scientific and ethical standards.
• You will be able to collect data from Phase I, II and III clinical trials within HDP programs and apply research methods
• You will be responsible for the presentation of scientific research results, research manuscripts and review articles (both internal and external)
• You will design, develop and maintain clinical databases and perform clinical data analysis
• You will prepare documentation in accordance with approval requirements and ICH-GCP
• You will coordinate clinical and non-clinical stakeholders, to ensure the smooth processing of documents and the conduct of studies
• You keep up to date with the latest developments in the relevant scientific literature
• You participate in translational scientific activities as well as projects in the field of clinical pharmacology

Please refer the Job description for details