Aya Healthcare is seeking a Clinical Research Coordinator

• Oncology for a 3 month contract role in East Brunswick, New Jersey! East Brunswick, NJ (100% Onsite) $40
• 43/hour 13-Week Contract Monday-Friday | 8:00 AM
• 5:00 PM Aya Healthcare is seeking an experienced Clinical Research Coordinator with oncology research experience to support a leading clinical research site in East Brunswick, NJ.

This is an excellent opportunity for an experienced research professional with a strong understanding of clinical trial coordination, GCP guidelines, and regulatory compliance.

Responsibilities:

Coordinate day-to-day activities for multiple oncology clinical trials while ensuring protocol compliance. Screen and enroll research participants according to study eligibility criteria. Facilitate the informed consent process and maintain accurate study documentation. Serve as the primary liaison between investigators, sponsors, CROs, and research staff. Maintain regulatory binders and essential study documents. Complete case report forms (CRFs), data entry, and resolve study queries. Assist with Serious Adverse Event (SAE) documentation and protocol deviations. Support study start-up, monitoring visits, and closeout activities. Ensure compliance with Good Clinical Practice (GCP), FDA regulations, and study protocols. Manage multiple active research protocols simultaneously while maintaining exceptional attention to detail.

Required Qualifications:

Minimum 2 years of Clinical Research Coordinator experience Oncology clinical research experience is

REQUIRED

Experience coordinating multiple active clinical trial protocols Experience with: Patient screening Informed consent Regulatory documentation Protocol compliance Study sponsor and CRO communication Working knowledge of Good Clinical Practice (GCP)

High School Diploma or GED Preferred Qualifications:

Early Phase (Phase I) Oncology clinical trial experience Associate's or Bachelor's degree Experience with OnCore and/or ARIA Experience using Clinical Trial Management Systems (CTMS)

Technical Skills:

Microsoft Office Suite Electronic Clinical Documentation Systems Clinical Trial Management Systems (CTMS)

Pay:

$40.00

• $43.

00 per hour

Benefits:

Dental insurance Health insurance Vision insurance

Education:

Associate (Required)

Experience:

Clinical research: 2 years (Required)

Oncology:

1 year (Required) (CTMS): 1 year (Required)

Good Clinical Practice:

1 year (Required) Oncology clinical research: 1 year (Required) Ability to

Commute:

East Brunswick, NJ 08816 (Required)

Work Location:

In person