This is a temporary position to support clinical research trials. A bonus will be paid on successful qualification of patients onto clinical trial studies Duties/Responsibilities: Manage the recruitment of subjects for study participation via methods including, but not limited to: database review, contacting prior patients, reaching out to patients identified by outreach or advertising, patients who have recently completed a previous study Develop and conduct pre-screen procedures utilizing sponsor/trial specific pre-screen questionnaire to evaluate potential eligibility for a clinical trial Responsible for developing a rapport with and providing excellent customer service to prospective patients Answer questions regarding participation in a clinical research trial including but not limited to fundamental of informed consent as well as general information regarding study procedures Enter and track subjects into the site’s clinical database ensuring accurate contact information and basic patient demographics Schedule subjects for on-site screening visits and collaborate with Site Director regarding staffing needs Evaluate necessary information from the research participants (i.e., HIPAA, Medical Chart Release Authorization, Questionnaires) and when applicable, medical records Understand the protocol (i.e., study timelines, inclusion and exclusion criteria, study requirements) Maintain, track, and perform quality checks on various site logs (i.e., study subject enrollment logs, pre-screen, and screening logs) as needed Attend community events to promote VelocityClinical Research and advertise for studies Track and assist in evaluating responses for individual patient outreach initiatives including but not limited to centralize advertising campaigns and local site-initiated campaigns to assist Site Director in determining success and ROI of campaign Maintain confidentiality of patient protected health information Other duties as assigned Required Skills/Abilities: Demonstrated knowledgeof medical terminology Proficient in the use of the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone. Ability to work in a fast-paced environment Strong verbal, written, and organizational skills Strong interpersonal and communication skills Ability to work as a team player Demonstrated abilityto read, write, and speak English Ability to multi-task Ability to followwritten guidelines Ability to work independently, plan and prioritize with minimal guidance Ability to be flexible/adapt as daily schedule may change rapidly Must be detail oriented Proficient problem solving and strategicdecision making ability. Proficient in accepting individual responsibility for actions taken and demonstrating professionalism when judged, critiqued and/or praised. Demonstrated leadership ability Be analytical with a strong focus on reporting and results to make informed data-driven recommendations and decisions A bonus will be paid on successful qualification of patients onto clinical trial studies