Malina Ruxandra Moisuc

-Participating in all phases of oncology studies, including feasibility assessments, start-up phase: ISA, SIV, recruitment, and closure visits.

-Performing on-site and off-site visits as per SMP.

-Guiding and mentoring new Clinical Trial Monitors.

Involved in multiple study stages, such as preparing sites for activation, submitting documents to the Ethics Committee, transitioning studies to EUCTR, preparing ICFs, managing Clinical Trial Package for CTMS, communicate with the study team to ensure all pending items are resolved for activation.

Working as CTA for Romania and Turkey, mentoring new CTAs, performing site payments, and managing site payments while participating in all study stages. This includes start-up activities like collecting documents, preparing the CTP and OSIF, and assisting site staff with system access, as well as overseeing maintenance and closure.

Organizing and overseeing administrative aspects of the Efficacy studies (necessary consumables and other materials needed, equipment);;Preparing of Efficacy studies: progress, preparation of examination room before start of studies, equipment verification;Acknowledge of different techniques of evaluation;

Filling of study documents (CRF and others study documents) and maintain study source documents; Report/summary/preliminary results write-up;Archiving of study documents at the end of the study."