Clinical Research Coordinator: Autoimmune Trials (Hybrid)

University Of Michigan; Ann Arbor (MI); Hybrid; USD 65,000 - 90,000; Full time

Benefits offered by this job

Excellent medical, dental and vision

2:1 retirement match

Job summary

University of Michigan is seeking an experienced Clinical Research Coordinator at the Intermediate level to support a longitudinal cohort of autoimmune disease studies and translational trials. You will work with a clinical research team and program manager to coordinate study start-up through close-out, including IRB submissions and consent processes.

You will oversee data management, sample handling, and participant visits while contributing to SOP development and training.

Qualifications

• Bachelor's degree in Health Science or an equivalent combination of related education and experience.
• Certification through ACRP (CCRC) or SoCRA (CCRP) or equivalent, with eligibility to register or take exam within six months of hire.
• IRB/Regulatory knowledge including initial submissions and amendments, with strong interpersonal and organizational skills.
• Ability to work independently with attention to detail and high organizational standards.
• Experience with data entry into eCRF systems (REDCap, iMedidata, etc.).
• Ability to collaborate with a multidisciplinary team in outpatient/inpatient settings and understand CFR, GCP, FDA regulations.

Responsibilities

• Coordinate multiple clinical studies from start-up to close-out in accordance with protocols and regulations.
• Prepare and submit IRB applications and informed consent documents.
• Screen and enroll eligible participants and obtain informed consent.
• Coordinate participant visits, assessments, and research activities per protocols.
• Coordinate collection, processing, storage, and shipment of study samples.
• Process participant payments and maintain documentation related to compensation.
• Develop and maintain SOPs and study-specific resources.
• Manage study data collection, entry, review, and reconciliation; resolve data queries.
• Serve as primary contact for participants, investigators, monitors, and stakeholders.
• Maintain accurate study records; support study closeout activities.

Skills

Independent worker

Excellent communication

Multitasking

Detail oriented

Record keeping

Education

Bachelor's degree in Health Science or related field

Tools

REDCap

iMedidata

EPIC

MiChart

eResearch systems

OnCore CTMS

Job description

University of Michigan is seeking an experienced Clinical Research Coordinator at the Intermediate level to support a longitudinal cohort of autoimmune disease studies and translational trials. You will work with a clinical research team and program manager to coordinate study start-up through close-out, including IRB submissions and consent processes.

You will oversee data management, sample handling, and participant visits while contributing to SOP development and training.