Clinical Research Coordinator II — Lead Complex Trials

Iterative Health; New Albany (IN); On-site; USD 55,000 - 75,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II (CRC II) to lead independent coordination of complex industry-sponsored trials across sites. The role involves enrollment, protocol adherence, patient safety, and close collaboration with investigators, sponsors, CROs, and internal teams.

You will manage visits, process specimens, ensure data integrity, and help drive enrollment success while maintaining regulatory compliance and high-quality study documentation.

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline required.
• 3–5 years of clinical research or healthcare experience required.
• CCR C or CCRP certification preferred or equivalent.
• Proficiency with CTMS, EDC systems, and standard office software applications.
• Familiarity with CTMS or EDC systems preferred.

Responsibilities

• Independently coordinate and manage industry-sponsored clinical trials from start-up through closeout.
• Manage complex visit schedules and protocol-related activities with adherence to timelines.
• Lead patient recruitment and retention including consent discussions and enrollment tracking.
• Conduct protocol-required patient visits and procedures per GCP and SOPs.
• Process lab specimens and prepare shipments according to protocol and regulations.
• Maintain study documentation, source records, and database updates.
• Ensure high-quality data entry and timely query resolution.
• Serve as a primary contact for study participants and coordinate with sponsors/CROs.

Skills

Organizational skills

Attention to detail

Prioritization

Communication

Education

Associate’s degree or Bachelor’s degree in a scientific/healthcare field

Tools

CTMS

EDC systems

Office software

Job description

Iterative Health is seeking a Clinical Research Coordinator II (CRC II) to lead independent coordination of complex industry-sponsored trials across sites. The role involves enrollment, protocol adherence, patient safety, and close collaboration with investigators, sponsors, CROs, and internal teams.

You will manage visits, process specimens, ensure data integrity, and help drive enrollment success while maintaining regulatory compliance and high-quality study documentation.