Assistant Clinical Research Coordinator

Responsibilities

• Monitor and ensure study data is collected following plan of care, guidelines and identified group resources
• Serve in rotation with assistant clinical coordinators and clinical research coordinators
• Serve as liaison between assigned clinical research coordinator and all clinical departments
• Participate in collaborative team efforts with other departments
• Discuss and administer Informed Consent Form
• Check and ensure that procedure areas are properly stocked with study supplies and equipment (i.e. blood tubes, kits, study flowsheets, ECG machines, BP cuffs, etc.)
• Assist assigned Clinical Research Coordinator review study schedules to ensure that study procedures are properly staffed
• Assist assigned Clinical Research Coordinator with the creation and/or review of study flowsheets to ensure study is conducted according to protocol requirements
• Anticipate, recognize, and resolve issues
• Reads and understands each protocol in which she/he is involve
• Follow established guidelines in the collection of clinical data and/or administration of clinical studies
• Performs all other duties as assigned
• Support adverse event reporting and informed consent administration
• Notify staff of abnormal results or incidents
• Ensure participant comfort and readiness for procedures
• Set up supplies and procedure areas per protocol
• Perform venipuncture, vital signs, ECG, and other assessments
• Communicate with participants to explain procedures and gather data
• Assist with patient care and emergency measures as needed
• Attend study initiation meetings and perform study-related tasks
• Provide high-quality care under pressure
• Maintains current licensure, registration and/or certification within educational background
• Maintains current BLS and/or ACLS certification
• Maintains necessary CEU’s for licensure, registration and/or certification
• Actively participates on CPMI’s ongoing Quality Assurance Program, HIPAA and Compliance Programs
• Keeps apprised of all new OSHA and GCP/ICH rules and regulations
• Attends all appropriate team meetings regarding study protocols
• Maintains skills in use of EKG machines, Holter hook-up and monitoring, diabetic monitoring and taking accurate vital signs
• Reads and understands CPMI policy and procedures manuals, SOP manual and employee handbook

Benefits

• Medical and dental coverage
• A matching 401(k)
• Paid time off to recharge
• Evolution Research Group is an independent clinical research site company in the U.S.
• Edison, New Jersey, USA
• https://ergclinical.com
• Late Stage
• Leadership Team
• Daniel Gruener
• Chief Medical Officer
• Recent News
• PR Newswire
• Evolution Research Group, LLC Appoints George Konis, MD, as President, Psychiatry and Addiction Research
• 2026-03-25
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Qualifications

• Maintains current licensure, registration and/or certification within educational background
• Maintains current BLS and/or ACLS certification
• Maintains necessary CEU's for licensure, registration and/or certification
• Maintains skills in use of EKG machines, Holter hook-up and monitoring, diabetic monitoring and taking accurate vital signs

Required skills

• BLS/ACLS Certification, Diabetic Monitoring, Electrocardiography (ECG), HIPAA Compliance, Holter Monitoring, ICH Guidelines, Venipuncture, Vital Signs Measurement

Experience

• Entry level