Clinical Research Associate II (m/f)
Michael Page
Lisboa, PT
há 4 dias
  • 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.
  • Great opportunity for your professional growth.

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