Clinical Trials Study Coordinator

Valley Health System

Paramus, Northern (NJ, KY)

Hybrid

USD 40,000 - 51,000

Full time

5 days ago
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Benefits offered by this job

Medical/Prescription, Dental & Vision
Retirement Plan
Tuition Assistance
Employee Assistance Program (EAP)
Fitness Center Membership Discount

Job summary

Valley Health System is seeking a Research Coordinator to coordinate clinical research activities under the Principal Investigator and Research Nurse Manager. You will assist in planning, consent subjects, schedule visits, and ensure protocol adherence and data quality.

The role requires a Bachelor’s degree or 10 years’ study coordination experience, plus related certifications and ongoing regulatory training.

Qualifications

  • Bachelor's degree or minimum ten years' experience as a study coordinator required.
  • 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 the PI and Research Nurse Manager.
  • Assist in project planning, coordinate and implement clinical research, ensure safety and accuracy of treatment per protocol.
  • Consent subjects when appropriate, schedule appointments and ancillary services, and register patients for billing and data collection.
  • Remain current in regulatory education, training and certification requirements.

Skills

English language proficiency
Strong communication
Time management

Education

Bachelor's degree
10 years' experience as study coordinator

Tools

Excel
Web-based databases

Job description

Valley Health System is seeking a Research Coordinator to coordinate clinical research activities under the Principal Investigator and Research Nurse Manager. You will assist in planning, consent subjects, schedule visits, and ensure protocol adherence and data quality.

The role requires a Bachelor’s degree or 10 years’ study coordination experience, plus related certifications and ongoing regulatory training.

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