Senior Clinical Research Coordinator: Trial Leadership

Iterative Health; Macon Township (MI); On-site; USD 80,000 - 110,000; Full time

Job summary

Iterative Health is seeking a Senior Clinical Research Coordinator to oversee complex industry-sponsored trials and mentor staff across multiple sites. You will manage start-up through closeout, coordinate visits, and ensure regulatory compliance, while driving enrollment and data quality.

Ideal candidates bring 5+ years in clinical research or healthcare, strong GCP/FDA knowledge, and experience mentoring junior staff.

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline required.
• 5+ years of clinical research or healthcare experience required.
• Must be able to perform blood draws, vital signs, and EKGs where allowed.
• CCRC/CCRP or equivalent certification strongly preferred.
• Strong understanding of GCP, FDA regulations, and clinical research operations.
• Experience mentoring or supporting junior staff.
• Proficiency with CTMS, EDC, and office software.

Responsibilities

• Lead and independently manage complex industry-sponsored trials from start-up to closeout.
• Coordinate visit schedules and protocol activities per timelines and regulations.
• Lead patient recruitment and retention initiatives.
• Mentor junior coordinators and staff on trial processes and sponsor communication.
• Ensure accurate study documentation and data queries resolution.
• Prepare for monitoring visits, audits, and inspections.
• Maintain study equipment inventory and supplies.

Skills

Clinical research

Mentoring

GCP & FDA regulations

CTMS/EDC proficiency

Communication skills

Organizational skills

Education

Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline

Tools

CTMS

EDC systems

Job description

Iterative Health is seeking a Senior Clinical Research Coordinator to oversee complex industry-sponsored trials and mentor staff across multiple sites. You will manage start-up through closeout, coordinate visits, and ensure regulatory compliance, while driving enrollment and data quality.

Ideal candidates bring 5+ years in clinical research or healthcare, strong GCP/FDA knowledge, and experience mentoring junior staff.