Summary:

For all clinical research studies assigned, the Clinical Research Coordinator (CRC) is responsible for
coordinating clinical research studies in a compliant and efficient manner. Under the direction of the
Principal Investigator (PI), the CRC will collaborate with all members of the clinical research team to
ensure all federal, state, university, and protocol requirements are followed, institutional research
objectives are met, and that ethical obligations are kept. This position will be primarily responsible for
the following duties as they relate to Huntington's Disease research projects, though the scope may
expand or change.

Core Responsibilities:

• Management of all duties required for clinical research studies from initiation to close-out.
• Conduct of clinical research activities as authorized by the Principal Investigator's documented
Delegation of Authority and Training Logs.
• On-call coverage for research projects as needed.
• Collaboration with department administrative staff and the School of Medicine Office of
Research Administration, coordination of the initiation processes for Movement Disorders
research projects and other clinical research projects in the Department of Neurology;
• Maintenance of current CITI credentials for Human Subjects Protections, Good Clinical Practice
(GCP), Clinical Research Coordinator, plus additional sponsor GCP certifications as required.
• Understanding and adherence to all IRB requirements, Human Subjects protection regulations,
and all aspects of IRB approved protocols.
• Conducting all assigned activities in compliance with national, local, & institutional guidelines,
according to all HIPAA, GCP, and other applicable requirements.
• Study activities including coordinating new study activation requirements, screening/enrolling
participants, regulatory and compliance requirements, maintaining appropriate study
documentation/records, and managing study data.