Clinical Research

• Provide direction, instruction and guidance to coordinate research activities including patient screening and recruitment, enrollment and education.
• Ensure protocol procedures have been completed adhering to Good Clinical Practice Guidelines as defined by the Federal Drug Administration (FDA) and serve as subject matter expert.
• Independently coordinate nursing/social work and patient care and/or patient follow-up functions of the clinical study including planning and developing related activities.
• Provide quality patient care to patients and their families within area of clinical specialty.
• Collaborate with care coordinators, social workers, psychologists, physicians and other appropriate treatment team members in diagnostic formulation, treatment direction, and recommendations.
• Act as a liaison with medical staff, university departments, ancillary departments and/or satellite facilities.
• Initiate and assist with developing and revising policies and procedures for nursing practice.
• Serve as a peer-mentor within the department, supporting management and in various responsibilities as appropriate including the development of less experienced team members.
• Contribute to the development of new processes, procedures, tools and training to enhance clinical research activities, compliance, and efficiency.
• Ensure compliance with contract principles, federal regulations, laws and UC/UCPC policy and operating procedures.
• Work closely with UC and UC Health offices in negotiation of contracts, confidentiality agreements and amendments related to the conduct of research activities.
• Independently work with necessary parties to identify compliance, legal, IP and business/financial risk.

Clinical Research Professional III, Neurology & Rehabilitation Medicine – Stroke

Clinical Research Project Manager, Radiology

Clinical Research Professional II, Neurology – Rehabilitation Medicine

Clinical Research Professional II, Radiology

Clinical Research Professional, Biorepository