Michigan Medicine
Clinical Research Technician/Assistant
Job Summary: This position may independently provide study coordination for simple and moderately complex clinical research studies. As a member of a coordination team, this position may help support a portfolio of projects with varying levels of complexity. Mastery of all job duties from the CRC-Assistant position on the Michigan Medicine CRC Career Ladder is required.
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. It 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.
Benefits
Excellent medical, dental and vision coverage effective on your first day
2:1 Match on retirement savings
Responsibilities Characteristic Duties and Responsibilities:
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
We are seeking a motivated clinical research professional who enjoys patient‑oriented, collaborative translational science and desires to contribute to research in a team‑based environment. The Clinical Research Coordinator will join the clinical research team within the growing Pediatric Diabetes Research Program at the University of Michigan.
Assist with recruiting, screening, consenting and enrolling research participants in our Pediatric Endocrinology clinics
Develop a prospective Type‑1 juvenile diabetic patient cohort and coordinate follow‑up visits for longitudinal cohorts
Perform clinical data entry, database management, and train staff in the collection of patient bio specimens and disease activity measures
Support the preparation for IRB audits and monitoring
Assist with developing and writing abstracts, manuscripts, and clinical trials protocols
Communicate with sponsors, IRB, and regulatory agencies regarding study progress, budgets, and compliance
Train other research staff and maintain accurate documentation
Supervision Supervision Received: This position receives direct supervision and reports to a CRC‑Lead, CRC‑Project Manager, or unit Administrator. Functional supervision may also be received from the Clinical Research Coordinator Senior in the team.
Supervision Exercised: None
Required Qualifications
Excellent interpersonal, oral, and written communication skills
Proficient computer skills including Microsoft software applications
Ability to organize/prioritize tasks effectively and efficiently
Demonstrated ability to manage work across various stakeholders
Ability to set goals, exercise sound professional judgment, and problem‑solve within delegated authority
Ability to work independently to meet milestones and deadlines
Solid attendance record and work ethics
Technician Level Requirements
Associate degree in Health Science or an equivalent combination of related education and experience (minimum 1 year of directly related experience in clinical research and clinical trials)
Advanced degree in a health‑related area such as Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, or a foreign MD
Minimum 3 years of human subject experience (clinical, lab, or health regulations)
Assistant Level Requirements
High school diploma or GED
Desired Qualifications
Bachelor's degree in Health Science or an equivalent combination of related education and experience
Understanding of medical terminology and experience in a large complex health care setting
Effective communication with staff and faculty of all levels, and knowledge of university policies and procedures
Experience in clinical research or clinical trials
Experience with the University of Michigan eResearch system
Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) certification
Experience in writing manuscripts and progress reports
Good judgment and strong problem‑solving skills related to clinical research experience
Knowledge of medical terminology
Familiarity with REDCap, OnCore, Epic, MiChart, and eResearch applications
Knowledge of UMHS policies and practices
Proven experience in administering IRB/regulatory requirements protocols
Work Schedule Full‑time, Monday‑Friday, 8‑hour shifts. Flexibility on weekends and evenings may be required depending on study needs.
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.
Underfill Statement This position may be underfilled at the CRC‑Assistant title based on selected candidates’ qualifications.
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.
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.
U‑M EEO Statement The University of Michigan is an equal employment opportunity employer.
Seniority level Entry level
Employment type Full‑time
Job function Research, Analyst, and Information Technology
Industries Hospitals and Health Care
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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. It 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.
Benefits
Excellent medical, dental and vision coverage effective on your first day
2:1 Match on retirement savings
Responsibilities Characteristic Duties and Responsibilities:
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
We are seeking a motivated clinical research professional who enjoys patient‑oriented, collaborative translational science and desires to contribute to research in a team‑based environment. The Clinical Research Coordinator will join the clinical research team within the growing Pediatric Diabetes Research Program at the University of Michigan.
Assist with recruiting, screening, consenting and enrolling research participants in our Pediatric Endocrinology clinics
Develop a prospective Type‑1 juvenile diabetic patient cohort and coordinate follow‑up visits for longitudinal cohorts
Perform clinical data entry, database management, and train staff in the collection of patient bio specimens and disease activity measures
Support the preparation for IRB audits and monitoring
Assist with developing and writing abstracts, manuscripts, and clinical trials protocols
Communicate with sponsors, IRB, and regulatory agencies regarding study progress, budgets, and compliance
Train other research staff and maintain accurate documentation
Supervision Supervision Received: This position receives direct supervision and reports to a CRC‑Lead, CRC‑Project Manager, or unit Administrator. Functional supervision may also be received from the Clinical Research Coordinator Senior in the team.
Supervision Exercised: None
Required Qualifications
Excellent interpersonal, oral, and written communication skills
Proficient computer skills including Microsoft software applications
Ability to organize/prioritize tasks effectively and efficiently
Demonstrated ability to manage work across various stakeholders
Ability to set goals, exercise sound professional judgment, and problem‑solve within delegated authority
Ability to work independently to meet milestones and deadlines
Solid attendance record and work ethics
Technician Level Requirements
Associate degree in Health Science or an equivalent combination of related education and experience (minimum 1 year of directly related experience in clinical research and clinical trials)
Advanced degree in a health‑related area such as Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, or a foreign MD
Minimum 3 years of human subject experience (clinical, lab, or health regulations)
Assistant Level Requirements
High school diploma or GED
Desired Qualifications
Bachelor's degree in Health Science or an equivalent combination of related education and experience
Understanding of medical terminology and experience in a large complex health care setting
Effective communication with staff and faculty of all levels, and knowledge of university policies and procedures
Experience in clinical research or clinical trials
Experience with the University of Michigan eResearch system
Association of Clinical Research Professionals (ACRP) or Society of Clinical Research Associates (SoCRA) certification
Experience in writing manuscripts and progress reports
Good judgment and strong problem‑solving skills related to clinical research experience
Knowledge of medical terminology
Familiarity with REDCap, OnCore, Epic, MiChart, and eResearch applications
Knowledge of UMHS policies and practices
Proven experience in administering IRB/regulatory requirements protocols
Work Schedule Full‑time, Monday‑Friday, 8‑hour shifts. Flexibility on weekends and evenings may be required depending on study needs.
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.
Underfill Statement This position may be underfilled at the CRC‑Assistant title based on selected candidates’ qualifications.
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.
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.
U‑M EEO Statement The University of Michigan is an equal employment opportunity employer.
Seniority level Entry level
Employment type Full‑time
Job function Research, Analyst, and Information Technology
Industries Hospitals and Health Care
#J-18808-Ljbffr