Clinical Research Coordinator

About the role

The Clinical Research Coordinator performs a vital role for the Division of Endocrinology, diabetes and Metabolism at the department of Medicine by coordinating various components of multiple clinical research studies at any time. This position reports to the principal investigators at the Endocrine division. Primary responsibilities of the Clinical Research Coordinator include but are not limited to:

• Undertake coordinating tasks of clinical research studies.
• Aid investigators in successful recruitment and retention of subjects.
• Guide day-to-day operations of assigned studies, assuring adherence to protocol.
• Generate accurate reports.
• Resolve queries in a timely manner.
• Maintain contact with Principal Investigator, monitoring agency, sponsor, and contracted vendors.
• Generate IRB approved materials for distribution to study subjects to promote project enrollment and retention of enrolled subjects.
• Oversee implementation of research studies, generation of qualitative and quantitative data and data collection forms and surveys.
• Manage the day-to-day operations of the assigned project including development and implementation of research procedures and systems.
• Assist Principal Investigator(s) with administration of clinical trial protocols, including obtaining informed consents and screening subjects, maintaining research records and research subject records, managing correspondence, researching medical records, recording data, and attending training sessions.

Responsibilities

The Clinical Research Coordinator undertakes coordinating tasks of clinical research studies, assists investigators in successful recruitment and retention of subjects, guides day-to-day operations of assigned studies, generates accurate reports, resolves queries in a timely manner, maintains contact with Principal Investigator, sponsors, and contracted vendors, generates IRB approved materials for distribution to study subjects, oversees implementation of research studies, manages the day-to-day operations of the assigned project, and assists Principal Investigators with administration of clinical trial protocols.

Requirements

The minimum qualifications for this position include a bachelor’s degree and 2 years of clinical research-related experience, or an equivalent combination of education and experience. Applicants must be familiar with clinical research procedures and methodology.

Qualifications

No preferred qualifications listed.

Benefits

The University at Buffalo offers a comprehensive benefits package that prioritizes your well-being and success to enhance every aspect of your life. Learn more about our benefits.

Schedule

This position is full-time with 37.5 hours per week.

Pay

The salary range for this position is $44,850 - $54,600.