Clinical Research Coordinator II: Patient Enrollment & Protocols

present of AI; Clifton (NJ); On-site; USD 60,000 - 90,000; Full time

Job summary

Iterative Health in Clifton, NJ, seeks a Clinical Research Coordinator II to run industry-sponsored trials from start-up to closeout with minimal supervision, covering patient recruitment, consent talks, protocol visits, vitals, and data entry. CTMS/EDC proficiency and careful record keeping are essential.

The role requires 3–5 years in clinical research or healthcare, strong organizational skills, and the ability to read and apply protocols.

Qualifications

• 3–5 years in clinical research or healthcare
• Organized and detail-oriented with strong record-keeping
• Ability to read and apply protocols correctly
• Experience in stomach, liver or heart research and a coordinator certification would help

Responsibilities

• Run industry-sponsored trials from start-up to closeout with minimal supervision
• Lead patient recruitment and consent talks; manage protocol visits and vitals
• Perform clinical tasks (ECGs, blood draws, other procedures) and ensure accurate lab shipping
• Maintain accurate source records and data entry in CTMS/EDC systems

Skills

Clinical research coordination

Patient recruitment

Data entry

Tools

CTMS

EDC

Job description

Iterative Health in Clifton, NJ, seeks a Clinical Research Coordinator II to run industry-sponsored trials from start-up to closeout with minimal supervision, covering patient recruitment, consent talks, protocol visits, vitals, and data entry. CTMS/EDC proficiency and careful record keeping are essential.

The role requires 3–5 years in clinical research or healthcare, strong organizational skills, and the ability to read and apply protocols.