Michigan Medicine
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 This position will serve as a Clinical Research Coordinator Intermediate in the Oncology Clinical Trial Support Unit (O‑CTSU) – Clinic Research Group at the Rogel Cancer Center. The role involves administrative study coordination and clinic support to faculty and research teams for the University of Michigan Rogel Cancer Center, an NCI‑Designated Comprehensive Cancer Center and a member of the National Comprehensive Cancer Network (NCCN). You will work with a diverse team of 150 clinical research professionals, contributing to early‑phase and phase III trials, while gaining education, training, career development and certification opportunities.
Benefits
Excellent medical, dental, and vision coverage effective on your first day
2:1 Match on retirement savings
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
Duties include:
Performs study procedures with accuracy.
Triages complex study concerns appropriately.
Manages increasing protocol complexity and volume efficiently.
Contributes to the development of processes and tools to capture data per ALCOA‑C principles.
Provides logistic and regulatory guidance on investigator‑initiated studies to ensure compliance with university and federal guidelines.
Provides administrative support for study activity, including subject reimbursement and payments.
Participates in training to maintain certification as a Clinical Research Professional.
Monitors site compliance with subject safety reporting, escalates issues, and develops tools to enhance subject safety during study conduct.
Applies regulatory requirements to control investigational product development processes.
This position reports directly to an O‑CTSU Manager and may provide limited functional supervision of staff within the CRC Career Ladder.
Required Qualifications
Bachelor’s degree in Health Science or an equivalent combination of education and experience.
Certification as a Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) required; eligible to register or take the exam at hire and must complete or pass within six months of hire.
Minimum three years of directly related experience in clinical research and trials.
Desired Qualifications
Six or more years of directly related experience.
Work Schedule Monday through Friday, core business hours. Occasionally evening or weekend work may be required to meet deadlines or support patient care.
Modes of Work Positions eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department and are reviewed annually.
Additional Information Michigan Medicine is committed to advancing inclusion, diversity, equity, accessibility, and belonging. We strive to create a work culture where each team member feels respected, valued, and safe.
Background Screening Michigan Medicine conducts background screening and pre‑employment drug testing on candidates upon acceptance of a contingent job offer, in compliance with the Fair Credit Report Act.
Application Deadline Job openings are posted for at least seven calendar days. The review and selection process may begin as early as the eighth day after posting.
EEO Statement The University of Michigan is an equal employment opportunity employer.
Job Details Seniority level: Mid‑Senior level. Employment type: Full‑time. Job function: Research, Analyst, and Information Technology. Industries: Hospitals and Health Care.
Location: Ann Arbor, MI. Salary: $33,000.00 – $38,700.00. Posting date: 2 months ago.
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Job Summary This position will serve as a Clinical Research Coordinator Intermediate in the Oncology Clinical Trial Support Unit (O‑CTSU) – Clinic Research Group at the Rogel Cancer Center. The role involves administrative study coordination and clinic support to faculty and research teams for the University of Michigan Rogel Cancer Center, an NCI‑Designated Comprehensive Cancer Center and a member of the National Comprehensive Cancer Network (NCCN). You will work with a diverse team of 150 clinical research professionals, contributing to early‑phase and phase III trials, while gaining education, training, career development and certification opportunities.
Benefits
Excellent medical, dental, and vision coverage effective on your first day
2:1 Match on retirement savings
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
Duties include:
Performs study procedures with accuracy.
Triages complex study concerns appropriately.
Manages increasing protocol complexity and volume efficiently.
Contributes to the development of processes and tools to capture data per ALCOA‑C principles.
Provides logistic and regulatory guidance on investigator‑initiated studies to ensure compliance with university and federal guidelines.
Provides administrative support for study activity, including subject reimbursement and payments.
Participates in training to maintain certification as a Clinical Research Professional.
Monitors site compliance with subject safety reporting, escalates issues, and develops tools to enhance subject safety during study conduct.
Applies regulatory requirements to control investigational product development processes.
This position reports directly to an O‑CTSU Manager and may provide limited functional supervision of staff within the CRC Career Ladder.
Required Qualifications
Bachelor’s degree in Health Science or an equivalent combination of education and experience.
Certification as a Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) required; eligible to register or take the exam at hire and must complete or pass within six months of hire.
Minimum three years of directly related experience in clinical research and trials.
Desired Qualifications
Six or more years of directly related experience.
Work Schedule Monday through Friday, core business hours. Occasionally evening or weekend work may be required to meet deadlines or support patient care.
Modes of Work Positions eligible for hybrid or mobile/remote work mode are at the discretion of the hiring department and are reviewed annually.
Additional Information Michigan Medicine is committed to advancing inclusion, diversity, equity, accessibility, and belonging. We strive to create a work culture where each team member feels respected, valued, and safe.
Background Screening Michigan Medicine conducts background screening and pre‑employment drug testing on candidates upon acceptance of a contingent job offer, in compliance with the Fair Credit Report Act.
Application Deadline Job openings are posted for at least seven calendar days. The review and selection process may begin as early as the eighth day after posting.
EEO Statement The University of Michigan is an equal employment opportunity employer.
Job Details Seniority level: Mid‑Senior level. Employment type: Full‑time. Job function: Research, Analyst, and Information Technology. Industries: Hospitals and Health Care.
Location: Ann Arbor, MI. Salary: $33,000.00 – $38,700.00. Posting date: 2 months ago.
#J-18808-Ljbffr