Job Summary – 3 open positions,
Experience and Education
- Bachelor’s degree in basic sciences, business administration, or related field and two (2) years research coordination experience.
-Participates in patient recruitment ensuring proper informed consent, eligibility requirements are met and enrolls patient onto trial.
-Manage patients on research study ensuring all study required visits are completed per protocol.
-Maintains compliance with protocol requirements and all applicable regulatory requirements.
-Performs accurate and complete data entry, case report form completion and query management.
-Maintains patient study binder per departmental guidelines including all related source documentation.
-Ensure data is entered into clinical trial monitoring systems.
-Appropriately utilizes the electronic medical record for management of the patient on study and to communicate with clinical staff.
-Participate in monitoring visits, site initiation visits and close-out visits as needed.
-Attends required training, maintains applicable certification and/or licensure as required.
-Attends regularly scheduled team meetings. Performs other duties as assigned
-Ensures regulatory compliance of clinical research program.
-Develops system for data collection and management of clinical research program registry information.
-Duties performed may include one or more of the following core functions: Directly interacting with or caring for patients, Directly interacting with or caring for human-subjects research participants,
-Train clinical research assistants.
-Performs other duties as assigned.
|Job Category||Lancaster / Desoto, TX, Rockwall / Wylie, TX, Waxahachie / Mansfield, TX|