Complies with Health and Safety Standards and Guidelines.
Ability to perform head-to-toe assessments on all patients and reassessments in compliance with the clinical research protocol.
Demonstrate an ability to assist physicians, principal investigator and sub-investigators with protocol-related procedures.
Demonstate an ability to be flexible, organized, detail-oriented, and function under stressful situations.
Knowledge of medications and their correct administration utilizing the clinical research protocol.
Follows protocol guidelines to ensure/reduce the potential of medication errors.
Performs all aspects of patient care in an environment that optimizes patient safety and reduces the likelihood of medical/health care errors and are in compliance with clinical research protocol.
Ability to interpret the results of waived tests; takes appropriate action on waived test results.
Treats patients and their families with respect and dignity.
Communicates appropriately and clearly to physicians, principal investigator, sub-investigators and staff and all others.
Demonstrates an ability to be flexible, organized and function under stressful stituations.
Documentation meets current standards and policies, including those governed by the FDA's Good Clinical Practices (GCP).
Consults with other departments as appropriate to collaborate in patient care and performance improvement activities with regard to patients' participation in a clinical trial