Katarzyna Olejnik

• Responsible for conducting all types of monitoring (pre-study, initiation, monitoring and close-out visits) of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors; site selection, contract negotiation
• Functions as the primary contact for sites regarding regulatory compliance and protocol questions and communicate with clinical sites on an ongoing basis to address and resolve all issues;
• Responsible for Preparing Clinical Trial Applications to the Regulatory Authorities and Ethics Committee;
• Provides support to Lead CRAs (monitoring reports review)
• Provides training to CRAs and CTAs;

• Responsible for conducting all types of monitoring (pre-study, initiation, monitoring and close-out visits) of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors; site selection, contract negotiation
• Functions as the primary contact for sites regarding regulatory compliance and protocol questions and communicate with clinical sites on an ongoing basis to address and resolve all issues;
• Responsible for Preparing Clinical Trial Applications to the Regulatory Authorities and Ethics Committee;