Clinical Research Coordinator I, Department of Neurology

Following detailed instructions by the supervisor, assist with promoting/recruiting research participants for long-term clinical trials. Participate in routine recruitment, screening, and enrollment of study participants who meet research eligibility criteria. Help obtain consent forms for approval by Human Subjects Panel. Maintain and update recruitment and screening materials, compliance forms, and tracking documents. Assist with collecting basic information, such as medical histories and assessments interviews, collect and process specimens, answer general questions, fill out case report forms, and help with telephone and in-person contact. Notifies Principal Investigator and supervisor of subject status. Under the direction of the PI and Senior lab members, assist with new protocol submissions, renewals, and revisions to Institutional Review Board for multiple studies. Aid in the submission of study protocols and amendments, consent forms, and recruiting materials to the Institutional Review Board and department for approval with oversight from supervisor. Provide assistance with collecting data, entering and analyzing data, and compiling reports, adhering to proper research protocols. Prepare basic documentation, reports, graphs, and other materials. Keep appropriate logs, tracks participants, and prepares study materials. Under direction of the PI and Senior lab members, assist with coordinating and carrying out daily operations including ordering/maintaining laboratory supplies/equipment. Attend lab meetings. Knowledge, Skills Abilities: Ability to manage multiple priorities, maintain accurate and detailed records, and meet deadlines in a fast-paced research environment. Strong written and verbal communication skills and proficiency with computer applications used for research documentation and data entry. Ability to work both independently and with a team, resolving issues with a positive outcome. Ability to maintain data accuracy, uphold research integrity, and perform work in accordance with ethical and compliance standards. Ability to contribute to the development of research programs, policies, and procedures and support continuous improvement.