The research coordinator is responsible for enlisting, maintaining and assuring protocol compliance for all patient on clinical trials. Collaborates with physician in determining eligibility of patients for clinical trials. Provides education to staff and patients.
Prepares for study initiation by gaining an in-depth knowledge of the protocol, developing patient recruitment plans, developing operations implementation plans for impact to care site resources.
Screens potential patients for protocol eligibility.
Presents trial concepts and derails to patients, participates in the informed consent process and reenrolls patients to study.
Coordinators patient care in compliance with protocol requirements.
May disburse investigational drug and maintains investigational drug accountability.
Responsible for reviewing protocol specific billing guides and submitting billing information to appropriate personnel.
Participates in data collection, entry and reporting for the subjects.
Located in Denver, CO.
One year of experience in clinical or scientific relations discipline
Two years of experience in a clinical or scientific related discipline and associate's degree may be substituted for the bachelor's degree.
Experience in Microsoft office
IATA Training and Certification
Experience working with physicians
Knowledge of FDA regulations and GCP
Experience in electronic medical record systems, clinical trial management systems, and electronic data capture systems
|Date Posted||June 10, 2018|
|Date Closes||July 10, 2018|
|Located In||Denver, CO|