Senior Human Subjects Research Coordinator — Clinical Trials

University of Rochester; City of Rochester (NY); On-site; USD 34,440 - 48,216; Full time

Job summary

University of Rochester seeks a motivated Human Subjects Research Coordinator II to manage neuromuscular disease studies, including observational and clinical trials. You will coordinate visits, ensure protocol compliance, and support Principal Investigators in a multi-site research setting.

The role requires a Bachelor's degree and 2+ years in human subject research coordination, with SOCRA/ACRP certifications preferred.

Qualifications

• Bachelor's degree required; experience in human subject research coordination preferred.
• Proficiency in word processing and data analysis software.
• Experience with Excel spreadsheets and electronic databases preferred.

Responsibilities

• Recruit, consent, enroll and retain study subjects across NMD portfolio.
• Coordinate study visits and maintain study documentation per protocol.
• Mentor HSRC I and supervise students as assigned.
• Manage IRB submissions, regulatory documentation and cross-site standardization.

Skills

Word processing

Data analysis

Excel

Education

Bachelor's degree

Job description

University of Rochester seeks a motivated Human Subjects Research Coordinator II to manage neuromuscular disease studies, including observational and clinical trials. You will coordinate visits, ensure protocol compliance, and support Principal Investigators in a multi-site research setting.

The role requires a Bachelor's degree and 2+ years in human subject research coordination, with SOCRA/ACRP certifications preferred.