University of Michigan
Clinical Research Coord Inter
Apply Now
How to Apply
A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.
Job Summary
The University of Michigan PET (Positron Emission Tomography) Imaging Center, housed in the Department of Radiology, is seeking a highly motivated and organized clinical research coordinator to join our team. This role will provide coordination for human research studies featuring the use of PET imaging technologies, potentially including other imaging modalities (e.g., SPECT, CT, MRI). The role will include primary coordination of studies led by investigators inside the PET Center. The person in this role will serve as a liaison to collaborating teams outside the department to help coordinate PET imaging procedures included in their research studies. As such, excellent interpersonal and organizational skills are required. Characteristic duties include significant contribution to the development and maintenance of study protocols, coordinating participant screening and scheduling for imaging studies, assisting with data collection and management, and serving as a resource on these topics to collaborating research groups.
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.
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
Responsibilities *
Expert level knowledge, skills, and abilities within all 8 competency domains is expected:
Scientific Concepts and Research Design
Ethical Participant Safety Considerations
Investigational Products Development and Regulation
Clinical Study Operations (GCPs)
Study and Site Management
Data Management and Informatics
Leadership and Professionalism
Communication and Teamwork
Day to day responsibilities of the role include:
Prepare and maintain regulatory documents for multiple research projects
Perform recruitment, screening, and enrollment of participants for imaging studies
Schedule imaging visits for study participants, often requiring coordination with multiple imaging teams
Assist with assessments and data collection
Orient collaborating coordinators to imaging-specific aspects of study screening, scheduling, and assessments
Assist with data management
Assist with regulatory and DSMB reports
May perform other duties as assigned.
Required Qualifications *
Bachelor's degree in Health Science or an equivalent combination of related education and experience.
Certification is required through Association of Clinical Research Professionals (ACRP) as a Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Association (SOCRA) as a Certified Clinical Research Professionals (CCRP) or equivalent. Candidates must be eligible to
register or take the exam
at date of hire and the certification must be
completed or passed etc.
within six months of date of hire. (Please review eligibility criteria from SoCRA or ACRP )
Minimum 3 years of directly related experience in clinical research and clinical trials is necessary.
Please review SoCRA's Definition of a Clinical Research Professional qualifying experience prior to applying.
Excellent verbal and written communication skills
Highly organized, detail-oriented, responsible, and responsive, with strict adherence to deadlines
Experience with regulatory document development and oversight
Ability to work independently and as a team member
Outstanding problem-solving skills and resourcefulness
Proficiency in Microsoft Word and Excel
Eagerness to learn new skills and take on new responsibilities
Desired Qualifications *
Experience with REDCap software
Work Schedule
Days, 40 hours per week.
Work Locations
Victor Vaughn
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 thework modes (https://hr.umich.edu/working-u-m/my-employment/ways-we-work-resource-center/ways-we-work-implementation-group/modes-work) .
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 employment opportunity employer.
Job Detail
Job Opening ID
263583
Working Title
Clinical Research Coord Inter
Job Title
Clinical Research Coord Inter
Work Location
Ann Arbor Campus
Ann Arbor, MI
Modes of Work
Onsite
Full/Part Time
Full-Time
Regular/Temporary
Regular
FLSA Status
Exempt
Organizational Group
Medical School
Department
MM Department of Radiology
Posting Begin/End Date
8/13/2025 - 10/12/2025
Career Interest
Radiology
Research
Apply Now
Apply Now
How to Apply
A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.
Job Summary
The University of Michigan PET (Positron Emission Tomography) Imaging Center, housed in the Department of Radiology, is seeking a highly motivated and organized clinical research coordinator to join our team. This role will provide coordination for human research studies featuring the use of PET imaging technologies, potentially including other imaging modalities (e.g., SPECT, CT, MRI). The role will include primary coordination of studies led by investigators inside the PET Center. The person in this role will serve as a liaison to collaborating teams outside the department to help coordinate PET imaging procedures included in their research studies. As such, excellent interpersonal and organizational skills are required. Characteristic duties include significant contribution to the development and maintenance of study protocols, coordinating participant screening and scheduling for imaging studies, assisting with data collection and management, and serving as a resource on these topics to collaborating research groups.
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.
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
Responsibilities *
Expert level knowledge, skills, and abilities within all 8 competency domains is expected:
Scientific Concepts and Research Design
Ethical Participant Safety Considerations
Investigational Products Development and Regulation
Clinical Study Operations (GCPs)
Study and Site Management
Data Management and Informatics
Leadership and Professionalism
Communication and Teamwork
Day to day responsibilities of the role include:
Prepare and maintain regulatory documents for multiple research projects
Perform recruitment, screening, and enrollment of participants for imaging studies
Schedule imaging visits for study participants, often requiring coordination with multiple imaging teams
Assist with assessments and data collection
Orient collaborating coordinators to imaging-specific aspects of study screening, scheduling, and assessments
Assist with data management
Assist with regulatory and DSMB reports
May perform other duties as assigned.
Required Qualifications *
Bachelor's degree in Health Science or an equivalent combination of related education and experience.
Certification is required through Association of Clinical Research Professionals (ACRP) as a Certified Clinical Research Coordinator (CCRC) or Society of Clinical Research Association (SOCRA) as a Certified Clinical Research Professionals (CCRP) or equivalent. Candidates must be eligible to
register or take the exam
at date of hire and the certification must be
completed or passed etc.
within six months of date of hire. (Please review eligibility criteria from SoCRA or ACRP )
Minimum 3 years of directly related experience in clinical research and clinical trials is necessary.
Please review SoCRA's Definition of a Clinical Research Professional qualifying experience prior to applying.
Excellent verbal and written communication skills
Highly organized, detail-oriented, responsible, and responsive, with strict adherence to deadlines
Experience with regulatory document development and oversight
Ability to work independently and as a team member
Outstanding problem-solving skills and resourcefulness
Proficiency in Microsoft Word and Excel
Eagerness to learn new skills and take on new responsibilities
Desired Qualifications *
Experience with REDCap software
Work Schedule
Days, 40 hours per week.
Work Locations
Victor Vaughn
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 thework modes (https://hr.umich.edu/working-u-m/my-employment/ways-we-work-resource-center/ways-we-work-implementation-group/modes-work) .
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 employment opportunity employer.
Job Detail
Job Opening ID
263583
Working Title
Clinical Research Coord Inter
Job Title
Clinical Research Coord Inter
Work Location
Ann Arbor Campus
Ann Arbor, MI
Modes of Work
Onsite
Full/Part Time
Full-Time
Regular/Temporary
Regular
FLSA Status
Exempt
Organizational Group
Medical School
Department
MM Department of Radiology
Posting Begin/End Date
8/13/2025 - 10/12/2025
Career Interest
Radiology
Research
Apply Now