• Recruiting potential investigators, preparing EC submissions, translating study-related documentation, organizing of meetings and other tasks as instructed by supervisor; • Completing Serious Adverse Event (SAE) reporting, processing production of reports;
• Assisting with training, mentoring, and development of new employees, e..g. co-monitoring.
• Basic understanding of the clinical trial process • Minimum two years of relevant clinical research experience in pharmaceutical or CRO industries • Thorough knowledge of ICH Guidelines and GCP including a basic understanding of
regulatory requirements. • Thorough knowledge of monitoring procedures.
• University Degree (life science) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology); • Fluency in English language.