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Under general supervision, coordinates clinical research study activity to screen, recruit, and enroll study participants; assists with IRB submissions; collects, evaluates and interprets data collected during clinical studies.
Knowledge of specialized medical/scientific terminology.
Knowledge of medication and proper dosages.
Exceptional organizational skills
Familiarity with basic protocol procedures
Prior exposure and interviewing of high risk participants
Attentiveness to detail
Interpersonal/human relations skills.
Written and verbal communication skills.
Ability to maintain confidentiality.
Ability to type and operate a personal computer.
Ability to analyze and interpret statistical data.
Associate’s degree or equivalent; supplemented with two to three (2-3) years of related experience. Certification in an area of specialty related to the study preferred.
Screens, recruits and enrolls study participants; confers with participants to explain purpose of study and obtain informed consent; administers injectible medication; coordinates clinical studies; obtains patient’s medical histories; attends investigation meetings.
Evaluates and interprets collected clinical data in conjunction with Principal Investigator as appropriate; prepares oral or written presentations or reports and analyses setting forth progress trends and provides recommendations or conclusions; and is responsible for reporting any adverse events or protocol violations to the IRB as required.
Completes IRB submissions such as renewals and amendments; performs data entry from information gathered from the study; performs data analysis to check the integrity of the data; assists with grant preparation and tracking.
Other duties as assigned.
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