Clinical Research Coord

The University of Rochester is one of the country's top-tier research universities. Our 158 buildings house more than 200 academic majors, more than 2,000 faculty and instructional staff, and some 9,300 students - approximately half of whom are women.

Learning at the University of Rochester is also on a very personal scale. Rochester remains one of the smallest and most collegiate among top research universities, with smaller classes, a low 9:1 student to teacher ratio, and increased interactions with faculty.

Location: School of Medicine & Dentistry

Opening: Full Time 40 hours Grade 051 Surgery Research

Schedule: 8AM-5PM

Job Summary: GENERAL PURPOSE:
Coordinate research studies focusing on Strong Memorial Hospital Trauma Unit patients, including patient recruitment, clinical data collection and analysis, and report preparation.

SPECIFIC RESPONSIBILITIES:
Site and Staff Preparation:
Develop in-depth understanding of study protocols and be able to meet protocol, regulatory, and good clinical practice requirements. Prepare and submit protocols, consent forms and related documents for Human Subjects Review and IRB approvals.

Recruit, screen, and consent patients; enroll tem in studies.

Collect clinical data, enter into database, coordinate with research results.

Study Documentation:
Maintain source documents and study databases. Complete clinical data report forms for NIH studies. Prepare reports.

Coordinate with research laboratory for blood cell preparation and isolation and with other lab protocols as directed by PIs.

QUALFICATIONS:
Bachelor's degree and some experience with laboratory or clinical research preferred. Candidate should have excellent communication and interpersonal skills plus strong organizational, writing, and computer skills. Proficiency with Microsoft Word and Excel are required. Outstanding interpersonal and communication skills, excellent organizational abilities, self motivation, and attention to detail are required.
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