Clinical Research Coordinator II — Study Operations

University of Rochester; Wilmot (AR); On-site; USD 52,000 - 73,000; Full time

Job summary

University of Rochester is seeking a clinical research coordinator to support planning and execution of cancer center studies at our Rochester, NY campus. You will assist in protocol implementation, data collection, and coordination with study teams to ensure participant safety and regulatory compliance.

The role requires a bachelor’s degree and strong organizational skills, with a focus on quality and collaboration across multiple sites and teams.

Qualifications

• Bachelor's degree required.
• 1 year of relevant experience preferred.
• Strong interpersonal and organizational skills are expected.

Responsibilities

• Assist in planning, coordinating, implementing, monitoring and evaluating clinical research studies.
• Support day-to-day operations and protocol implementation.
• Coordinate study activities and data entry, ensuring regulatory compliance.
• Maintain logs and data quality; support audits and safety oversight.
• Communicate effectively with team, sponsor, and sites to ensure participant safety.

Skills

MS Office

Interpersonal communication

Team collaboration

Education

Bachelor's degree

Tools

MS Office

Job description

University of Rochester is seeking a clinical research coordinator to support planning and execution of cancer center studies at our Rochester, NY campus. You will assist in protocol implementation, data collection, and coordination with study teams to ensure participant safety and regulatory compliance.

The role requires a bachelor’s degree and strong organizational skills, with a focus on quality and collaboration across multiple sites and teams.