On-Site CRC: Enrollment & Compliance

Forefront Dermatology; Michigan; On-site; USD 60,000 - 75,000; Full time

Job summary

Forefront Dermatology in Grand Rapids, Michigan, is seeking a Clinical Research Coordinator to drive strategy and execution across assigned studies, ensure regulatory compliance, and deliver performance on enrollment, data quality, and protocol execution.

This 100% on-site role requires collaboration with sponsors, investigators, and CROs; the candidate will mentor staff and support protocol development while maintaining audit readiness and participant engagement.

Qualifications

• Bachelor's degree required.
• Experience interpreting regulations and maintaining audit readiness.
• Ability to analyze performance metrics and improve enrollment and data quality.
• Strong communication with sponsors, investigators, and leadership.

Responsibilities

• Direct clinical research operations across protocols and ensure regulatory standards are met.
• Oversee regulatory documentation and safety reporting; maintain audit readiness.
• Drive enrollment strategies, optimize screening and enrollment workflows.
• Coordinate with sponsors, investigators, and CROs to support study feasibility and site selection.
• Mentor team members and reinforce protocol standards across sites.
• Evaluate new opportunities and provide recommendations for protocol development.

Skills

Regulatory compliance

Independent judgment

Data analysis

Communication skills

Education

Bachelor's Degree

Job description

Forefront Dermatology in Grand Rapids, Michigan, is seeking a Clinical Research Coordinator to drive strategy and execution across assigned studies, ensure regulatory compliance, and deliver performance on enrollment, data quality, and protocol execution.

This 100% on-site role requires collaboration with sponsors, investigators, and CROs; the candidate will mentor staff and support protocol development while maintaining audit readiness and participant engagement.