-Monitoring and site management for phase I-IV;
-Measure the progress of clinical projects at the assigned investigative/physician sites (either on site or remotely);
-Ensure clinical projects are conducted, recorded and reported in accordance with the protocol;
-Evaluate the overall performance of site and site staff, providing recommendations regarding site-specific actions;
-Understand projects scope, budgets and timelines, managing site-level activities to ensure the project objectives and timelines are met;
-Act as the primary liaison with study site personnel;
-Prepare and attend Investigator Meetings and sponsor meetings;
-Perform all tasks routinely and independently, seeking guidance as needed.
-Degree in Health Sciences, such as training in Clinical Trials;
-2 years of experience in prior clinical research or monitoring;
-Experience in Oncology and Immunology;
-Knowledge of Regulatory requirements;
-Ability to easily adapt to new technologies;
-Excellent communication, presentation and interpersonal skills;
-Highly responsible, dedicated and with initiative;
-Ability to travel on a regular basis.