Clinical Research Coordinator (NJ) Job Description

Work Location: Mercer County, New Jersey

Summary:

The Clinical Research Coordinator oversees the daily operations of clinical trials, focusing on oncology studies. This role ensures protocol compliance, manages subject enrollment, and supports all aspects of clinical trial execution in a regulated environment.

Responsibilities:

• Coordinate and manage all aspects of clinical trial operations, including subject screening, enrollment, and follow-up.
• Ensure strict adherence to study protocols, regulatory requirements, and informed consent processes.
• Develop and implement subject recruitment strategies to meet study enrollment goals.
• Prepare and maintain study documentation, including charts, binders, and accountability logs.
• Perform delegated protocol-specific tasks, such as phlebotomy and equipment calibration, as required.
• Document study procedures, adverse events, and medication changes accurately and promptly.
• Communicate effectively with investigators and clinical staff regarding study drug administration and imaging procedures.
• Assist with monitoring visits, address action items, and ensure timely reporting of serious adverse events and protocol deviations.

Qualifications:

• Minimum High School Diploma or GED required.
• At least 5 years of US-based clinical research coordinator experience (foreign experience not counted).
• Oncology clinical research experience is required.
• Phlebotomy/blood draw skills strongly preferred.
• Certification from ACRP or SOCRA preferred.

Published Category: Clinical Operations & Development