Clinical Research Coordinator Washington DC Pay from: $27 Per hour MUST: 2+ years of experience as a Clinical Research Coordinator Strong patient facing experience Ability to determine if patients meet inclusions for study Experience recruiting and enrolling patients into Clinical Research Studies Experience explaining Informed Consent to patients and reviewing paperwork Experience with regulatory paperwork Strong medical terminology knowledge Experience recognizing and documenting adverse events Ability to follow proper clinical research protocols Experience utilizing clinical trial software as well as EMR Bachelors Degree DUTIES: The Duties of the Clinical Research Coordinator include but are not limited to the following: Respond to hospital alerts and determine if patients meet inclusions for studies and are eligible to be enrolled clinical research trials Recruit and enroll patients in clinical research studies Review paperwork and forms with patients Review Informed Consent Process with participants and document in the Source Department- Clinical Research System Discuss study protocols with participants and provide patient education Participate in meetings to review study Document appropriate information in case report forms and review data against with medical records to ensure accuracy Document and report adverse events Quadrant is an affirmative action/equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, status as a protected veteran, or status as an individual with a disability. Healthcare benefits are offered to all eligible employees according to compliance mandated by the Affordable Care Act.
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