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.
- Assist study team with aspects of clinical research coordination including: identifying potential subjects, screening subjects, consenting and enrolling subjects, and collecting and managing patient data for clinical research subjects.
- Communicate with study team and investigators concerning progress of research, subject related problems, recruitment strategies, and specific policies and procedures.
- Serve as key resource to research participants and collaborators. Work collaboratively by maintaining a good rapport and communication with research teams and faculty, as well as patients and families.
- Prepare and organize space for study related materials and equipment. Maintain study equipment and supplies.
- Staff members are expected to work independently and regularly exercise good judgment in setting priorities, resolving operational problems, and applying policies, procedures, and methods, while maintaining the strictest of confidentiality at all times.
- Other duties as required or assigned.
- Bachelor’s degree in a science or health-related field, or equivalent education and experience.
- 2-3 years of experience as a study coordinator, researcher or study monitor.
- Demonstrated understanding of clinical research; understand compliance issues related to human subjects research, knowledge and application of the Code of Federal Regulations (CFR), Good Clinical Practice (GCP), and FDA regulations.
- Demonstrated understanding of medical terminology.
- Excellent interpersonal, oral, and written communication skills with meticulous attention to detail.
- Proficient computer skills including Microsoft software applications.
- Ability to organize and manage multiple tasks simultaneously as well as prioritize and manage time and exercise good judgment.
- Ability to work independently with minimal supervision and with diverse teams of people in a diplomatic, collaborative and effective manner.
- Good attendance record.
- ACRP or SoCRA certification or effort towards certification.
- PEERS, CITI or NIH Protection of Human Subjects Training Certification as well as HIPAA Certification or willingness to meet this requirement.
8:00 AM - 4:30 PM
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.
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 openings are posted for a minimum of seven calendar days. This job may be removed from posting boards and filled anytime after the minimum posting period has ended.
U-M EEO/AA Statement
The University of Michigan is an equal opportunity/affirmative action employer.