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Clinical Research Coordinator
2 weeks ago
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
Bachelor's 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".
