Clinical Research Coordinator I

Position Description :

Summary

Perform the day-to-day administrative activities of the clinical research trials program in Neurosciences. Provide support to the team to facilitate the achievement of the program's goals.

Primary Responsibilities

• Recruit, screen, enroll and obtain consent from program participants. Conduct or coordinate training for program participants.
• Coordinate research protocols including arranging necessary appointments and procedures, working collaboratively with other departments and institutions, and maintaining contact with study participants.
• Collect, analyze, and disseminate program data. Report program data and progress to program stakeholders.
• Assist with study sample collection and processing.
• Identify problems or obstacles in the system / procedures related to implementation of the research protocols and communicate to the study investigators.
• Assure compliance with all relevant IRB and other regulatory agency requirements.
• Assist in the preparation of IRB documents and reports. Assist in the evaluation and writing of research protocols.
• Collaborate on the development of program materials including educational materials, marketing materials, websites, forms, and reports.
• Work with Principal Investigator to develop, implement, and maintain comprehensive databases and files related to the program.
• Maintain program timeline including tracking deadlines for program components.
• Coordinate program outreach activities including acting as a liaison with community organizations.
• Other duties as assigned.

Knowledge - Skills - Abilities

Preferred Schedule :

Position Requirements :

Qualifications

Appropriate experience may be substituted on equivalent basis.

Minimum Required Education : Associate's Degree

Minimum Required Experience : 1 year

Required Certification / Licensure(s) : CITI training within 90 days of hire

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