Senior Urology Clinical Trials Coordinator

001 University of Rochester; City of Rochester (NY); Sur place; USD 61 000 - 85 000; Plein temps

Résumé du poste

University of Rochester is seeking a Clinical Research Coordinator to support the Urology Clinical Trials Office. The role involves coordinating visits, collecting data, and ensuring protocol adherence across multiple sites in Rochester, NY.

The position requires a Bachelor's degree and 5 years of human subject coordination experience, plus strong interpersonal and organizational skills. Travel to affiliated sites may be necessary.

Qualifications

• Bachelor's degree and 5 years of experience in human subject coordination required.
• Knowledge of clinical research coordination, regulatory processes, and good clinical practices is expected.
• Strong interpersonal, data collection, and written communication skills.

Responsabilités

• Coordinate and conduct clinical study visits and assessments per protocol.
• Perform phlebotomy, sample collection, and data entry into databases.
• Identify eligible subjects, obtain consent, and enroll participants; monitor for adverse events.
• Prepare study documents, reports, and liaise with sponsors, IRBs, and site staff.

Connaissances

Phlebotomy

Interpersonal skills

Oral & written communication

Attention to detail

Problem solving

Computer skills

Formation

Bachelor's degree

5 years experience in human subject coordination

Outils

eRecord

ePARC

Excel

Description du poste

University of Rochester is seeking a Clinical Research Coordinator to support the Urology Clinical Trials Office. The role involves coordinating visits, collecting data, and ensuring protocol adherence across multiple sites in Rochester, NY.

The position requires a Bachelor's degree and 5 years of human subject coordination experience, plus strong interpersonal and organizational skills. Travel to affiliated sites may be necessary.