As a Trainee Clinical Research Associate, you'll provide support with site preparedness, logistical support to the monitoring process, and assist with assigned tasks for site management and remote monitoring in accordance with SOPs and regulatory guidelines
Job Summary
As a Trainee Clinical Research Associate, you'll provide support with site preparedness, logistical support to the monitoring process, and assist with assigned tasks for site management and remote monitoring in accordance with SOPs and regulatory guidelines.
You will complete study and site management activities, complete and document study-specific training, and orient and train on CRG/study-specific systems.
Responsibilities include supporting site staff with vendor qualification, coordinating study/site supply management, and performing reconciliation tasks on assigned trials.
Matching Summary
As a Trainee Clinical Research Associate, you'll provide support with site preparedness, logistical support to the monitoring process, and assist with assigned tasks for site management and remote monitoring in accordance with SOPs and regulatory guidelines.