Human Subjects Research Coordinator I - Clinical Studies

001 University of Rochester; United States; On-site; USD 30,000 - 43,000; Full time

Job summary

The University of Rochester is seeking a Human Subject Research Coordinator to support clinical studies at UR Medical Center in Rochester, NY. The role focuses on coordinating study activities, recruitment, and data management in accordance with Good Clinical Practice.

Responsibilities include screening participants, coordinating materials, training staff on protocol details, and liaising with sponsors, IRB, and study teams to ensure compliance and timely study progress.

Qualifications

• Bachelor's degree or Associate degree with trainee program completed or equivalent.
• Prior experience as a Phlebotomist preferred.
• Familiarity with Good Clinical Practice guidelines.

Responsibilities

• Coordinate activities for human subject research and study materials.
• Assist in recruitment and screening of participants.
• Train staff on protocol details and adverse event reporting.
• Liaise with sponsor monitors and IRB as needed.
• Ensure data are collected and stored per approved procedures.

Skills

Data analysis

Word processing

Education

Bachelor's degree or Associate's degree with trainee program

Job description

The University of Rochester is seeking a Human Subject Research Coordinator to support clinical studies at UR Medical Center in Rochester, NY. The role focuses on coordinating study activities, recruitment, and data management in accordance with Good Clinical Practice.

Responsibilities include screening participants, coordinating materials, training staff on protocol details, and liaising with sponsors, IRB, and study teams to ensure compliance and timely study progress.