Contract Clinical Research Coordinator - Onsite Growth

Profound Research LLC; Detroit (MI); On-site; USD 45,000 - 52,000; Full time

Job summary

Profound Research LLC in Detroit, MI is seeking a Clinical Research Coordinator to manage trial activities under supervision in compliance with ICH-GCP and study protocols.

The role requires a bachelor’s or associate degree with relevant life science experience, GCP certification goals, and strong attention to detail for patient visits, data collection, and regulatory documentation. On-site work with daily site travel is expected.

Qualifications

• Bachelor’s degree or higher with life science experience.
• Certification in GCP and CCRP/CCRC within 6 months.
• Experience performing clinical assessments and vital signs.

Responsibilities

• Conduct and manage trial activities per protocol and regulations.
• Complete required training including ICH-GCP and IATA.
• Mentor staff in trial conduct and management.
• Lead start-up, recruitment, data collection, and adverse event reporting.
• Ensure good documentation practices across trial records.
• Communicate with sponsors, CROs, and vendors.
• Travel daily to site(s) and manage supplies.

Skills

Clinical Research

GCP Certification

CCRC Certification

Data collection

Regulatory compliance

Communication

Team collaboration

Education

Bachelor’s degree

Associate’s degree

High School diploma / technical degree

Tools

GCP software tools

Job description

Profound Research LLC in Detroit, MI is seeking a Clinical Research Coordinator to manage trial activities under supervision in compliance with ICH-GCP and study protocols.

The role requires a bachelor’s or associate degree with relevant life science experience, GCP certification goals, and strong attention to detail for patient visits, data collection, and regulatory documentation. On-site work with daily site travel is expected.