Clinical Research Coordinator
2+years of experience as a Clinical Research Coordinator
Experience recruiting patients for trials and educating patients on how trials work
Experience with maintaining regulatory documents as well as Informed Consent process
Experience working with sponsors
Ability to maintain regulatory documents
Experience developing budgets for studies
Experience compiling data
Knowledge of protocol compliance and adverse event reporting
Bachelor's Degree is a Must
The Duties of the Clinical Research Coordinator include but are not limited to the following:
Ensure protocol compliance on clinical trials.
Determine eligibility of patients for clinical trials.
Screen potential patients for trials and educate patients on how trials work
Enroll patients and participates in the informed consent process
Coordinate patient care
Monitor patients for adverse events
Collect data and handle documentation and reporting of
Schedules and participates in monitoring and auditing activities.
Maintain regulatory documents in accordance with regulations
Compiling data and reporting protocol activity
*Quadrant, Inc. is an equal opportunity and affirmative action employer. Quadrant is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.