Neuromuscular Research Study Coordinator II

University of Rochester; City of Rochester (NY); On-site; USD 34,632 - 48,546; Full time

Job summary

The Neuromuscular Disease Study Coordinator II at University of Rochester Neurology coordinates observational studies and multi-center clinical research in adult and pediatric subjects, with emphasis on recruitment, consent, and protocol compliance.

You will mentor study coordinators, manage IRB submissions, oversee data integrity, and collaborate with sponsors and cross‑functional teams to advance milestones and ensure high-quality, compliant research.

Qualifications

• Bachelor's degree and 2 years of experience in human subject research coordination.
• Experience with Excel spreadsheets and electronic databases preferred.
• Knowledge of Good Clinical Practice, federal/state policies and SOPs.
• SOCRA/ACRP certification preferred.

Responsibilities

• Uses independent judgment to recruit, consent, enroll, and retain study subjects across the NMD portfolio.
• Coordinates study visits, ensures milestones, and supports protocol objectives.
• Mentors HSRC I and supervises students as assigned.
• Manages IRB submissions, amendments, and continuing reviews; maintains regulatory files.
• Collaborates with cross-functional teams, sponsors, and sites; monitors budgets and data integrity.

Skills

Word processing

Data analysis

Excel

Education

Bachelor's degree in a related field

Tools

OnCore

Job description

The Neuromuscular Disease Study Coordinator II at University of Rochester Neurology coordinates observational studies and multi-center clinical research in adult and pediatric subjects, with emphasis on recruitment, consent, and protocol compliance.

You will mentor study coordinators, manage IRB submissions, oversee data integrity, and collaborate with sponsors and cross‑functional teams to advance milestones and ensure high-quality, compliant research.