Lead CRC II; Onsite - Euless, TX

Overview

Updated: January 21, 2026
Location: Morrisville, NC, United States
Job :

Illingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries. These include mobile research nursing, patient concierge, medical photography and clinical research services. Illingworth are experts with experience across all study phases and in a diverse range of therapeutic areas. Illingworth Research Group is a global organization operating in over 45 countries, bringing clinical research directly into the home of the patient, to improve the experience of patients involved in clinical trials and the quality of their lives.

• Clinical Research Project Planning and Preparation
• Review of assigned protocols and other protocol documentation (ICF, IB) for accuracy, feasibility, timing, and resources.
• Prepare and maintain the Investigator Site File and/or Trial Master File (TMF) for the study.
• Participate in creation and review of timelines and start-up meetings (Investigator Meeting/SIV, Sponsor discussions, or other related meetings).
• Take the lead and/or overall coordination of all required start-up activities including, but not limited to:
  • Clinic logistics planning, schedule of clinic activities, and team training.
  • Preparation, review, and/or finalization of clinic source documents, time and events tables, and other required study materials; review of Case Report Forms (CRFs), laboratory workbooks, staff requirements, and schedules.
  • In collaboration with the responsible teams, establishes and/or maintains safety assessment requirements, Quality Control (QC) and monitoring plans, pharmacy/dispensing requirements, study supplies/equipment, meal plans, and other elements as applicable to the study.
  • Confirms all required regulatory and contractual documentation is present prior to study start.
• Support the Principal Investigator as needed with study related tasks such as:
  Delegation of Authority Log; management of daily tasks; visit calendar development and maintenance; scheduling and attending monitor visits.
• Advertise, recruit, and screen potential participants for the study.
• Clinical Conduct – Perform all study activities following Good Clinical Practices (GCP). Manage multiple clinical trials simultaneously. Protect the safety of human subjects. Monitor ongoing regulatory updates and enter study data; complete Case Report Forms; facilitate audits; develop patient and team rapport to minimize protocol violations; respond to auditor inquiries.
• Take the lead and/or overall coordination of clinic activities including supervising clinic visits, eligibility screening, and drug administration as delegated; ensure activities comply with protocol, SOP, and applicable regulations.
• Review and manage clinic updates, adverse event (AE) or serious adverse events (SAEs) reporting, study logs, quality control, and monitor findings.
• Post-Clinic/Close-Out Activities – Coordinate resolution of findings, close-out of study documentation, TMF updates, return of study supplies, IRB reports, and archiving as applicable. Monitor subject compliance and prepare for sponsor/monitor/QA audits. Provide status updates and participate in process improvement activities.
• Accommodate a flexible schedule (days, afternoons, nights, weekends) and perform other duties as assigned.

• Registered Nurse and/or University Degree (Bachelor of Science) required.
• Clinical Research certification preferred.
• Minimum 1 year of experience in clinical research required; 2+ years preferred, preferably in coordination of clinical research projects.
• Good knowledge of regulations, ICH GCP, privacy, and applicable guidelines.
• Required skills:
  
  problem solving, planning, and evaluation; strong time management, attention to detail, and ability to multi-task.
• Good interpersonal and communication skills with a team focus; knowledge of SOP writing; ability to anticipate problems and provide timely solutions; ability to coordinate multiple projects with competing deadlines.
• Proficiency in Word, Excel, PowerPoint; proficiency with clinical trial EDC software preferred; prior…