Clinical Research Coordinator II

001 University of Rochester; Wilmot (AR); Vor Ort; USD 52.000 - 73.000; Vollzeit

Zusammenfassung

The University of Rochester is seeking a Clinical Research Coordinator to support cancer center trials at the Rochester campus. You will coordinate enrollment, data collection, and regulatory compliance, working closely with study teams, sponsors, and participants to ensure protocol adherence.

Applicants should have a Bachelor's degree with 1 year of relevant experience and be proficient in MS Office. Strong communication and organizational skills are essential to succeed in a collaborative

Qualifikationen

• Bachelor's degree and 1 year of relevant experience or equivalent.
• Ability to understand and follow standard research protocols.
• Strong interpersonal, communication, and organizational skills.

Aufgaben

• Assist in planning, coordinating, implementing, monitoring, and evaluating clinical research studies.
• Assist in day-to-day operations and protocol implementation.
• Assist in study coordination from initiation to close-out according to regulatory/sponsor guidelines.
• Assure overall integrity of studies and adherence to standards and procedures.
• Coordinate with study team and other sites to ensure participant safety and protocol compliance.
• Maintain study logs, data collection tools, and research records.

Kenntnisse

MS Office

Communication

Team collaboration

Research coordination

Ausbildung

Bachelor's degree

Tools

OnCore

EMR systems

Jobbeschreibung

The University of Rochester is seeking a Clinical Research Coordinator to support cancer center trials at the Rochester campus. You will coordinate enrollment, data collection, and regulatory compliance, working closely with study teams, sponsors, and participants to ensure protocol adherence.

Applicants should have a Bachelor's degree with 1 year of relevant experience and be proficient in MS Office. Strong communication and organizational skills are essential to succeed in a collaborative