Clinical Research Coordinator II: Efficient Trial Execution

TAU Ventures; Troy (MI); On-site; USD 60,000 - 85,000; Full time

Job summary

Iterative Health is a healthcare technology and services company advancing clinical research to improve patient outcomes. We are looking for a Clinical Research Coordinator II to coordinate daily trial activities and ensure protocol adherence, regulatory compliance, and patient safety.

You will work closely with investigators, sponsors, CROs, and internal teams across multiple therapeutic areas to ensure successful study execution and enrollment targets.

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.
• Experience in gastroenterology, hepatology, or cardiology preferred.
• CCRC® or CCRP® or equivalent certification preferred.
• Strong organizational skills and attention to detail.

Responsibilities

• Independently coordinate and manage industry-sponsored clinical trials from start-up through closeout with minimal supervision.
• Lead patient recruitment and retention efforts including chart review, outreach, informed consent discussions, and enrollment tracking.
• Conduct protocol-required patient visits and assessments per protocol, GCP, and SOPs.
• Maintain accurate study documentation: source records, informed consent, CRFs, and CTMS updates.
• Maintain inventory of study equipment, supplies, and investigational products onsite.

Skills

Clinical research experience

Organizational skills

Effective communication

GCP / regulatory literacy

CTMS familiarity

EDC familiarity

Multi-stakeholder coordination

Education

Bachelor's degree

Associate's degree

Tools

CTMS

EDC

Office software

Job description

Iterative Health is a healthcare technology and services company advancing clinical research to improve patient outcomes. We are looking for a Clinical Research Coordinator II to coordinate daily trial activities and ensure protocol adherence, regulatory compliance, and patient safety.

You will work closely with investigators, sponsors, CROs, and internal teams across multiple therapeutic areas to ensure successful study execution and enrollment targets.