Clinical Research Specialist II - Study Coordination

University of Rochester; City of Rochester (NY); Hybrid; USD 3,463,000 - 4,855,000; Full time

Job summary

The University of Rochester is actively seeking a Clinical Research Specialist II to support the Cancer Center/Clin Trials Office. This full-time role assists in planning, coordinating, implementing, monitoring, and evaluating clinical studies per sponsor guidelines.

Responsibilities include enrolling participants, coordinating visits, managing data, and ensuring quality checks while maintaining regulatory standards and participant safety.

Qualifications

• Bachelor's degree and 1 year of relevant experience required.
• Ability to understand and follow protocol and data integrity standards.
• Strong interpersonal, communication, and organizational skills preferred.
• Strong interpersonal, communication, and organizational skills.
• Proficient in MS Office and related software.

Responsibilities

• Coordinates enrollment of participants in moderate risk/moderately complex studies.
• Handles recruitment activities, screening, and eligibility checks for candidates.
• Plans study timelines, schedules appointments and visits.
• Maintains case report forms, source documents, and research records.
• Entrants data into study databases and performs data quality checks.
• Ensures adherence to safety, regulatory guidelines and study procedures.

Skills

MS Office proficiency

Team collaboration

Attention to data integrity

Communication skills

Organizational skills

Education

Bachelor's degree

Tools

MS Excel

Data entry systems

Job description

The University of Rochester is actively seeking a Clinical Research Specialist II to support the Cancer Center/Clin Trials Office. This full-time role assists in planning, coordinating, implementing, monitoring, and evaluating clinical studies per sponsor guidelines.

Responsibilities include enrolling participants, coordinating visits, managing data, and ensuring quality checks while maintaining regulatory standards and participant safety.