Clinical Research Coordinator (CRC)

System One, Inc.; Riverdale (NJ); On-site; USD 52,000 - 76,000; Full time

Job summary

System One is seeking an experienced Clinical Research Coordinator for an onsite, full-time contract-to-hire position in Riverdale, New Jersey. The role requires coordinating day-to-day trial operations, including participant visits, consent, and documentation, with travel to nearby sites as needed.

The candidate will perform blood draws, specimen processing, and injections within clinical qualifications and ensure compliance with GCP, FDA regulations, and sponsor protocols.

Qualifications

• Minimum 1–3 years of clinical research experience, preferably in a patient-facing CRC position.
• GCP training/certification required.
• Human Subjects Protection training required, with proof of completion or verifiable CITI account.
• Must be comfortable independently drawing blood and processing clinical specimens.
• Experience with patient screening, informed consent, study visits, protocol compliance, and documentation.

Responsibilities

• Coordinate clinical research studies from screening through study completion.
• Review study protocols, inclusion/exclusion criteria, and participant eligibility.
• Conduct informed consent discussions and coordinate participant enrollment.
• Schedule and conduct study visits in accordance with protocol requirements.
• Manage patient follow-up, retention, and study documentation.
• Perform blood draws and process biological samples.
• Administer injections within the scope of the candidate's clinical qualifications.
• Prepare, handle, and document biological specimens.
• Support investigational product dispensing and accountability, as applicable.
• Maintain accurate source documentation and study records.
• Ensure adherence to GCP, FDA regulations, IRB requirements, and sponsor protocols.
• Document and elevate adverse events and serious adverse events.
• Coordinate with Principal Investigators, sponsors, and clinical operations teams.
• Assist with monitoring visits, data clarification, and protocol amendments.

Skills

Bilingual English/Spanish

Education

LPN or Certified Medical Assistant background

Bachelor's degree preferred

Tools

CTMS

Electronic source documentation

Clinical research databases

Job description

Job Title: Clinical Research Coordinator
Location: Riverdale, New Jersey
Type: Contract To Hire
Work Model: Onsite
Hours: M-F 8:30am-5:30pm

Overview

We are looking for an experienced Clinical Research Coordinator to support day-to-day clinical trial operations at an onsite research site in Riverdale, NJ, with travel to nearby locations. This full-time contract-to-hire role requires independent coordination of participant visits and documentation while also performing blood draws, specimen processing, and injections (within the scope of clinical qualifications).

Responsibilities

• Coordinate clinical research studies from screening through study completion.
• Review study protocols, inclusion/exclusion criteria, and participant eligibility.
• Conduct informed consent discussions and coordinate participant enrollment.
• Schedule and conduct study visits in accordance with protocol requirements.
• Manage patient follow-up, retention, and study documentation.
• Perform blood draws and process biological samples.
• Administer injections within the scope of the candidate's clinical qualifications.
• Prepare, handle, and document biological specimens.
• Support investigational product dispensing and accountability, as applicable.
• Maintain accurate source documentation and study records.
• Ensure adherence to GCP, FDA regulations, IRB requirements, and sponsor protocols.
• Document and elevate adverse events and serious adverse events.
• Coordinate with Principal Investigators, sponsors, and clinical operations teams.
• Assist with monitoring visits, data clarification, and protocol amendments.

Requirements

• Minimum 1–3 years of clinical research experience, preferably in a patient-facing CRC position.
• Current Good Clinical Practice training/certification required.
• Human Subjects Protection training required, with proof of completion or verifiable CITI account.
• Must be comfortable independently drawing blood and processing clinical specimens.
• Experience with patient screening, informed consent, study visits, protocol compliance, and documentation.
• Reliable transportation and willingness to travel between nearby clinical sites.
• LPN or certified Medical Assistant background.
• Bilingual English/Spanish, preferred.
• Experience working in community-based clinical research or physician practice settings.
• Familiarity with CTMS, electronic source documentation, and clinical research databases.
• IATA training/certification for handling and shipping biological specimens.
• Phlebotomy certification is a plus.
• Bachelor's degree preferred but not required.

System One, and its subsidiaries including Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

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Ref: #568-Clinical