Clinical Trials Research Coordinator

RWJBarnabas Health

Livingston (NJ)

On-site

USD 53,000 - 76,000

Full time

38 hours ago
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Benefits offered by this job

PTO
Medical and Prescription DrugInsurance
Dental and Vision Insurance
Retirement Plans
Disability Insurance
Life Insurance
Tuition Reimbursement
Wellness Programs
Voluntary Benefits
Discounts Through Partners

Job summary

RWJBarnabas Health is seeking a Research Coordinator to join our Research Department in Livingston, NJ. The role focuses on coordinating clinical studies, ensuring regulatory compliance, and supporting trial activities in a fast-paced hospital setting.

A strong background in health sciences, data management, and patient-centered care is essential. We offer growth opportunities, comprehensive benefits, and a collaborative clinical research environment.

Qualifications

  • Must have a Bachelor's degree in a health-related field or equivalent.
  • Strong problem-solving, critical thinking, and collaboration skills.
  • Ability to multitask, manage time effectively, and work with minimal supervision.
  • Proficiency in Microsoft Office applications and related software tools.
  • Prior clinical research or patient care experience preferred.
  • Active CITI training is preferred.

Responsibilities

  • Coordinate clinical research studies from pre-activation through close-out.
  • Manage participant recruitment, screening, enrollment, and retention.
  • Maintain regulatory documents, IRB submissions, budgets, and invoices.
  • Use electronic data capture systems and trial management software.
  • Monitor enrollment, data quality, and compliance with GCP and ALCOA.

Skills

Communication
Attention to detail
Healthcare informatics
Team collaboration

Education

Bachelor's degree in health science or related

Tools

MS Office Suite

Job description

RWJBarnabas Health is seeking a Research Coordinator to join our Research Department in Livingston, NJ. The role focuses on coordinating clinical studies, ensuring regulatory compliance, and supporting trial activities in a fast-paced hospital setting.

A strong background in health sciences, data management, and patient-centered care is essential. We offer growth opportunities, comprehensive benefits, and a collaborative clinical research environment.

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