Clinical Research Coordinator (CRC)

System One Clinical & Science is seeking a Clinical Research Coordinator to support day-to-day clinical trial operations at an onsite research site. The role coordinates participant visits and study documentation, performs blood draws and specimen processing, and supports compliance with study protocols and regulatory requirements.

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 escalate adverse events and serious adverse events
• Coordinate with Principal Investigators, sponsors, and clinical operations teams
• Assist with monitoring visits, data clarification, and protocol amendments

Preferred

• preferably in a patient-facing CRC position
• Bilingual English/Spanish, preferred
• Phlebotomy certification is a plus
• Bachelor's degree preferred
• Patient-Facing CRC Experience
• Bilingual English/Spanish
• Phlebotomy Certification
• Bachelor’s Degree

Benefits

• Eligible employees: health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, and voluntary plans
• Eligible employees: participation in a 401(k) plan

Company

• Professional staffing for clinical, scientific, and healthcare organizations
• Edison, New Jersey, USA
• http://jouleinc.com/
• Founded in 1965
• 51-200 employees

Qualifications

• Minimum 1–3 years of clinical research experience
• 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
• LPN or certified Medical Assistant background
• 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
• Preferably in a patient-facing CRC position
• Bilingual English/Spanish, preferred
• Phlebotomy certification is a plus
• Bachelor's degree preferred

Required skills

• Clinical Research Coordination, Clinical Research Documentation, Clinical Specimen Processing, Clinical Trial Management Systems (CTMS), Clinical Trial Protocol Compliance, Electronic Source Documentation, English and Spanish, Human Subjects Protection, IATA Biological Specimen Handling and Shipping, Informed Consent, LPN or Certified Medical Assistant, Patient Screening, Phlebotomy

Preferred skills

• Bachelor's degree preferred, Bilingual English/Spanish, preferred, Phlebotomy certification is a plus, preferably in a patient-facing CRC position

Experience

• 1-3 years