Research Study Coordinator I – Regulatory & Participant Ops

CHEManager International; Detroit (MI); On-site; USD 60,000 - 75,000; Full time

Job summary

CHEManager International in Detroit, MI seeks a Clinical Research Coordinator to oversee research projects under minimal supervision, ensuring regulatory compliance and CFR guidelines. The role provides technical support to Principal Investigators and coordinates day-to-day study operations.

The candidate will engage with participants and internal/external stakeholders, manage recruitment, and offer additional support as needed.

Qualifications

• Bachelor's degree in a scientific field (Psychology, Sociology, Anthropology or related).
• SOCRA or ACRP certification preferred; IATA certification also noted.

Responsibilities

• Coordinate research projects with adherence to regulatory compliance and CFR guidelines.
• Provide technical support to Principal Investigators.
• Interact with internal and external customers at all levels; oversee recruitment and day-to-day study operations.
• Direct contact with potential and enrolled study participants is expected.
• Provide other support as required.

Skills

Research experience

Good communication

Reliable transportation

Phlebotomy useful

Education

Bachelor's degree in science

Certifications: SOCRA/ACRP

Job description

CHEManager International in Detroit, MI seeks a Clinical Research Coordinator to oversee research projects under minimal supervision, ensuring regulatory compliance and CFR guidelines. The role provides technical support to Principal Investigators and coordinates day-to-day study operations.

The candidate will engage with participants and internal/external stakeholders, manage recruitment, and offer additional support as needed.