Senior CRC: Lead Complex Trials & Mentor Teams

MD Ally; Dayton (OH); On-site; USD 65,000 - 90,000; Full time

Job summary

Iterative Health seeks a Senior Clinical Research Coordinator to oversee complex industry-sponsored trials, mentor staff, and ensure regulatory compliance. The role focuses on study start-up to closeout, patient engagement, and data integrity.

You will coordinate scheduling, conduct protocol-driven visits, and support site performance while maintaining GCP adherence and sponsor communications.

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 draw, vital signs, and EKGs as applicable by state law.
• CCRC® or CCRP® certification strongly preferred.

Responsibilities

• Lead and independently manage complex industry-sponsored clinical trials from study start-up through closeout.
• Coordinate complex study visit schedules and protocol-related activities while ensuring regulatory compliance.
• Lead patient recruitment and retention initiatives to support enrollment performance.
• Mentor and support junior coordinators and research staff on clinical trial processes and sponsor communication.
• Maintain accurate study documentation and ensure data quality and regulatory readiness.

Skills

Clinical research experience

Mentoring

Regulatory compliance

Communication skills

CTMS/EDC proficiency

Education

Bachelor’s/Associate degree in science or healthcare

Tools

CTMS

EDC systems

Job description

Iterative Health seeks a Senior Clinical Research Coordinator to oversee complex industry-sponsored trials, mentor staff, and ensure regulatory compliance. The role focuses on study start-up to closeout, patient engagement, and data integrity.

You will coordinate scheduling, conduct protocol-driven visits, and support site performance while maintaining GCP adherence and sponsor communications.