Clinical Research Study Coordinator — Patient Advocate

Valley Medical Services Inc; Paramus (NJ); On-site; USD 61,000 - 76,000; Full time

Job summary

Valley Health System is seeking a Study Coordinator to coordinate and administer research study activities under the Principal Investigator and Research Nurse Manager. The role includes planning, implementing clinical research, and advocating for patient safety and protocol adherence.

Responsibilities include consenting subjects, scheduling appointments and ancillary services, billing data registration, and ensuring accuracy of the treatment regimen.

Qualifications

• Bachelor's degree or minimum ten years' study coordinator experience.
• CPR, Phlebotomy, IATA and CCRP or CCRC certification upon hire or to be obtained as appropriate.
• Maintains CITI certification and ongoing knowledge of ICH-GCP.

Responsibilities

• Coordinate and administer research study activities under PI and Research Nurse Manager.
• Assist in project planning; coordinate and implement clinical research.
• Consent subjects when appropriate and schedule appointments and ancillary services.
• Register patients for billing compliance and data collection; ensure safety, consistency and accuracy of treatment regimens.

Skills

Medical terminology

Time management

English communication

Education

Bachelor's degree

CCRP/CCRC certification

CITI certification

CPR/Phlebotomy

Tools

Excel

Web-based databases

Data entry

Job description

Valley Health System is seeking a Study Coordinator to coordinate and administer research study activities under the Principal Investigator and Research Nurse Manager. The role includes planning, implementing clinical research, and advocating for patient safety and protocol adherence.

Responsibilities include consenting subjects, scheduling appointments and ancillary services, billing data registration, and ensuring accuracy of the treatment regimen.