Clinical Research Coordinator II: Trials Data & Compliance

Dm Clinical Research Group; Monitor Charter Township (MI); On-site; USD 55,000 - 75,000; Full time

Job summary

Dm Clinical Research Group in the United States is seeking a Clinical Research Coordinator II to ensure quality research at assigned sites in accordance with sponsor protocol, FDA regulations, and ICH-GCP guidelines.

The role focuses on meeting enrollment expectations, training completion, data entry accuracy, and strong communication with investigators and sponsor/CRO teams at the site level.

Qualifications

• Must have strong attention to detail and be able to multi-task across studies.
• Excellent written and verbal communication skills in English; bilingual English/Spanish preferred.
• Experience as a CRC or similar coordination role in industry-sponsored studies is a plus.

Responsibilities

• Conduct study visits and perform protocol-required procedures; document findings promptly.
• Enter data and resolve queries per sponsor and company guidelines.
• Maintain ALCOA-C compliant documentation and knowledge of FDA/ICH-GCP guidelines.
• Support recruitment and retention efforts at assigned sites to meet enrollment goals.
• Communicate with investigators, staff, participants, and sponsor representatives; report adverse events per policy.
• Assist with site initiation, monitoring visits, and audits; prepare for Investigator Meetings.
• Obtain informed consent and ensure patient understanding of procedures and risks.

Skills

Attention to detail

Multi-tasking

Communication skills

Bilingual English/Spanish

Education

High School Diploma or equivalent

Bachelor's degree preferred

Tools

EDC systems

IVRS

Job description

Dm Clinical Research Group in the United States is seeking a Clinical Research Coordinator II to ensure quality research at assigned sites in accordance with sponsor protocol, FDA regulations, and ICH-GCP guidelines.

The role focuses on meeting enrollment expectations, training completion, data entry accuracy, and strong communication with investigators and sponsor/CRO teams at the site level.