Clinical Research Coord Assoc

Michigan Medicine; Ann Arbor (MI); On-site; USD 52,000 - 78,000; Full time

Benefits offered by this job

Health insurance (medical, dental, and

Retirement matching (2:1)

Job summary

Michigan Medicine at Kellogg Eye Center is seeking a coordinator to onsite coordinate moderate to complex clinical research studies, manage IRB submissions, and oversee participant recruitment and data collection, including vision assessments and surveys.

The role requires knowledge of Good Clinical Practice and IRB processes, and at least 1 year of direct clinical research participant interaction, with ability to collaborate across multidisciplinary teams.

Qualifications

• Experience with human subjects research and GCP.
• Familiarity with IRB processes.
• Minimum 1 year direct clinical research participant interaction.

Responsibilities

• Collects and maintains patient data for clinical research projects.
• Screens and oversees recruitment of study participants.
• Coordinates scheduling of experiments, procedures, and visits.
• Manages data collection, processing, and analysis in line with study protocols.
• Monitors subjects for safety and compliance.
• Completes IRB documentation with PI support.

Skills

GCP knowledge

IRB processes

Clinical research

Data collection

Participant interaction

Tools

REDCap

Job description

Mission Statement

Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Our mission is guided by our Strategic Principles and has three critical components; patient care, education and research that together enhance our contribution to society.

Job Summary

Works onsite at the Kellogg Eye Center coordinating moderate to complex clinical research studies, managing associated IRB applications, and overseeing and participating in participant recruitment and data collection, which may include vision assessments, imaging studies, motor assessments, neurocognitive testing and survey completion.

Responsibilities

Collects and maintains patient data for clinical research projects. Screens and oversees recruitment of study participants. Coordinates scheduling of experiments, procedures, and visits. Manages data collection, processing, and analysis in line with study protocols. Monitors subjects for safety and compliance. Completes IRB applications and associated documentation with PI support. Collaborate swith clinical decision support teams and stakeholders to ensure consistent system standards.

Required Qualifications

Proficiency in human subjects research protocols,Good Clinical Practice(GCP),and regulatory compliance. Knowledge of the IRB application process relevant to clinical research in academic medicine. At least 1 year of experience in direct clinical research participant interaction.

Desired Qualifications

Strong organizational and time-management skills.

Ability to work in dependently and collaborate effectively with multidisciplinary teams.

Experience with electronic data capture systems and research databases including REDCap.

Experience with scientific writing.

Basic knowledge of ophthalmology/eyecare

Why Join Michigan Medicine?

Michigan Medicine is one of the largest health care complexes in the world and has been the site of many groundbreaking medical and technological advancements since the opening of the U-M Medical School in 1850. Michigan Medicine is comprised of over 30,000 employees and our vision is to attract, inspire, and develop outstanding people in medicine, sciences, and healthcare to become one of the world?s most distinguished academic health systems. In some way, great or small, every person here helps to advance this world-class institution. Work at Michigan Medicine and become a victor for the greater good.

What Benefits can you Look Forward to?

• Excellent medical, dental and vision coverage effective on your very first day
• 2:1 Match on retirement savings

Modes of Work

Positions that are eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department. Work agreements are reviewed annually at a minimum and are subject to change at any time, and for any reason, throughout the course of employment. Learn more about the work modes.

Work Schedule

This position involves a standard Monday-Friday, 40-hour work week. Remote work may be available when being onsite is not necessary for patient testing or recruitment.

Background Screening

Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act. Pre-employment drug testing applies to all selected candidates, including new or additional faculty and staff appointments, as well as transfers from other U-M campuses.

Application Deadline

Job openings are posted for a minimum of seven calendar days. The review and selection process may begin as early as the eighth day after posting. This opening may be removed from posting boards and filled anytime after the minimum posting period has ended.

U-M EEO Statement

The University of Michigan is an Equal Opportunity Employer. We are committed to providing an environment of mutual respect where equal employment opportunities are available to all applicants, including protected veterans and individuals with disabilities.