Clinical Research Coordinator ; Clinic - Medical Oncology

Benefits

Responsibilities

• •Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants;
• •resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency
• •Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner
• •Ensures timely completion of all protocol requirements (assessment, lab testing, procedures and treatments), to include scheduling and facilitating the patient’s timely completion of protocol requirements; evaluates and interprets collected clinical data as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions of the same
• •Collects clinical data under clinical research protocols
• •Performs other duties as assigned
• •Up to 22 days of vacation, 10 recognized holidays, and sick time
• •Take advantage of our free Metro transit U-Pass for eligible employees
• •5 more items(s)