Hybrid Clinical Research Technician – Study Coordination

University of Michigan Information and Technology Services; Ann Arbor (MI); Hybrid; USD 42,000 - 60,000; Full time

Benefits offered by this job

Excellent medical, dental and vision

2:1 retirement match

Job summary

Michigan Medicine invites applications for a Clinical Research Technician to independently coordinate studies of varying complexity. You will be part of a CRC team, support portfolio management, and ensure adherence to GCPs, IRB submissions, and data integrity.

The role emphasizes collaboration with study teams, sponsors, and regulatory bodies while maintaining strict confidentiality and professional standards. Hybrid work and a strong focus on patient data integrity are offered.

Qualifications

• Associate’s Degree or equivalent in combined education and clinical research experience.
• Minimum of 1+ years direct related experience OR advanced degree in health-related areas OR 3 years of related human subjects experience.
• Underfill with High School Diploma or GED if applicable.

Responsibilities

• Provide study coordination for simple and moderately complex clinical research studies.
• Support a portfolio of projects with varying levels of complexity.
• Assist in IRB submissions, safety reporting and regulatory communications.
• Identify potential subjects, screen, consent and enroll, and collect data for studies.
• Prepare and organize study materials, data and specimens; monitor results and documentation.
• Collaborate with sponsors, IRB, and university officials; maintain confidentiality and quality.

Skills

Clinical research

Study coordination

IRB submissions

Data management

Education

Associate’s Degree or equivalent in combined education and clinical research experience

Bachelor’s Degree in Health Science or equivalent

Tools

OnCore

Epic

MiCHART

eResearch

Job description

Michigan Medicine invites applications for a Clinical Research Technician to independently coordinate studies of varying complexity. You will be part of a CRC team, support portfolio management, and ensure adherence to GCPs, IRB submissions, and data integrity.

The role emphasizes collaboration with study teams, sponsors, and regulatory bodies while maintaining strict confidentiality and professional standards. Hybrid work and a strong focus on patient data integrity are offered.