• Facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study
• Administer sponsor required questionnaires
• Creates, manages, and maintains source documents for each trial
• Attends teleconferences and Investigator Meetings as requested by research director
• Reviews and comprehends all study protocols, e.g., study proceedings and timelines, inclusion and exclusion criteria, confidentiality and privacy protections
• Works with other members of the study team and clinical team to recruit eligible candidates to meet enrollment goals
• Screens subjects for eligibility using protocol-specific inclusion and exclusion criteria, documenting each potential participant's eligibility accurately
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