Senior Clinical Research Coordinator II - End-to-End Trials

Seae Ventures; Clifton (NJ); On-site; USD 65,000 - 90,000; Full time

Job summary

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities and ensure protocol compliance and patient safety across multiple sites. You will collaborate with patients, investigators, sponsors, CROs, and internal teams to drive high-quality trial execution.

The role emphasizes managing visits, screenings, informed consent, data capture, and documentation, with a focus on gastroenterology, hepatology, obesity, and cardiology trials.

Qualifications

• Associate’s or Bachelor’s degree in a scientific/healthcare field.
• 3–5 years of clinical research or healthcare experience.
• Experience in gastroenterology, hepatology, or cardiology preferred.

Responsibilities

• Coordinate and manage industry-sponsored clinical trials from start-up through closeout with minimal supervision.
• Lead patient recruitment and retention, including chart reviews and informed consent discussions.
• Conduct protocol-required visits, assessments, and procedures per GCP and SOPs.
• Maintain study documentation, data entry, and respond to data queries on timelines.

Skills

Clinical coordination

Attention to detail

Communication skills

Multitasking

Study coordination

Education

Bachelor's degree in scientific/healthcare field

Associate’s degree in scientific field

Tools

CTMS

EDC systems

MS Office

Job description

Iterative Health is seeking a Clinical Research Coordinator II to independently coordinate daily study activities and ensure protocol compliance and patient safety across multiple sites. You will collaborate with patients, investigators, sponsors, CROs, and internal teams to drive high-quality trial execution.

The role emphasizes managing visits, screenings, informed consent, data capture, and documentation, with a focus on gastroenterology, hepatology, obesity, and cardiology trials.