Senior Clinical Research Specialist - Urology Trials

University of Rochester; New York (NY); On-site; USD 61,000 - 85,000; Full time

Job summary

The University of Rochester seeks a Clinical Research Coordinator to support Urology clinical trials, overseeing study visits, data collection, and regulatory compliance. You will work with Strong Hospital, Highland Hospital, and outpatient clinics to ensure high-quality patient care and data integrity.

Responsibilities include phlebotomy, subject recruitment, and collaboration with the research team to maintain study documentation and quality assurance.

Qualifications

• Bachelor’s degree and 5 years of experience in human subject coordination required.
• Phlebotomy skills for adult and pediatric patients.
• Strong interpersonal and communication skills.
• Proficient in data collection, entry, and basic QA.

Responsibilities

• Participate in ongoing research studies in the Urology Clinical Trials Office; perform clinical research procedures (blood draws, etc.) and data collection.
• Identify eligible subjects, obtain informed consent, and manage enrollment procedures; support visits and sample handling.
• Collaborate with study team; maintain documentation, source data verification and regulatory compliance.
• Conduct QA activities to ensure study integrity and adherence to protocols; support sponsor and IRB interactions.
• May supervise staff and travel to off-site locations as required by study needs.

Skills

Phlebotomy

Interpersonal skills

Attention to detail

Computer proficiency

Education

Bachelor’s degree in a related field

SOCRA Certification (preferred)

ACRP Certification (preferred)

Tools

eRecord system

Microsoft Excel

Job description

The University of Rochester seeks a Clinical Research Coordinator to support Urology clinical trials, overseeing study visits, data collection, and regulatory compliance. You will work with Strong Hospital, Highland Hospital, and outpatient clinics to ensure high-quality patient care and data integrity.

Responsibilities include phlebotomy, subject recruitment, and collaboration with the research team to maintain study documentation and quality assurance.