Clinical Research Coordinator II — Lead Independent Trial Execution

Iterative Health; Clifton (NJ); Sur place; USD 65 000 - 90 000; Plein temps

Résumé du poste

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

The role requires 3-5 years of clinical research or healthcare experience, with preferred familiarity in gastroenterology, hepatology, or cardiology, and a CRC/CCRP certification is a

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline.
• 3-5 years of clinical research or healthcare experience.
• Experience in gastroenterology, hepatology, or cardiology is preferred.

Responsabilités

• Coordinate industry-sponsored clinical trials from start-up to closeout.
• Manage visit schedules and protocol-related activities to meet timelines.
• Lead patient recruitment, consent discussions, and enrollment tracking.

Connaissances

Clinical research

Coordination

Regulatory compliance

Communication

CTMS/EDC

Formation

Bachelor's/Associate degree

Outils

CTMS

EDC Systems

Description du poste

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

The role requires 3-5 years of clinical research or healthcare experience, with preferred familiarity in gastroenterology, hepatology, or cardiology, and a CRC/CCRP certification is a