Clinical Research Coordinator II - Pregnancy Studies

001 University of Rochester; United States; On-site; USD 35,000 - 49,000; Full time

Job summary

University of Rochester is seeking a full-time Research Coordinator to conduct clinical research in Obstetrics & Gynecology. You will recruit, screen and interview participants, collect data and specimens, perform data entry, and manage study visits to ensure protocol adherence.

Responsibilities include subject tracking, coordinating with the PI and sponsor, and maintaining study documents. A Bachelor's degree and 2 years of coordination experience are required; phlebotomy experience is a plus,

Qualifications

• Bachelor's degree and 2 years of experience in human subject research coordination required.
• Experience as a Phlebotomist preferred.
• SOCRA Certification upon hire or Association of Clinical Research Professionals experience preferred.

Responsibilities

• Recruit and screen potential study candidates and perform interviews.
• Data collection, chart reviews, data entry, and specimen handling.
• Coordinate study visits and ensure compliance with protocols.
• Maintain positive communication with study team, PI, and sponsor.
• Oversee subject tracking and regulatory documentation.

Skills

Recruitment

Data entry

Interviews

Teamwork

Detail oriented

Education

Bachelor's degree

Tools

Microsoft Office

Web-based database

Job description

University of Rochester is seeking a full-time Research Coordinator to conduct clinical research in Obstetrics & Gynecology. You will recruit, screen and interview participants, collect data and specimens, perform data entry, and manage study visits to ensure protocol adherence.

Responsibilities include subject tracking, coordinating with the PI and sponsor, and maintaining study documents. A Bachelor's degree and 2 years of coordination experience are required; phlebotomy experience is a plus,