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.