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Crc Ii (Hybrid) - Dallas/Euless, Tx

1-3 years
USD 67,700 – 115,100
10 Nov. 27, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Research Coordinator II (Hybrid) – Dallas/Euless, TX

Location: USA – Texas (Hybrid)
Job ID: 25103662
Updated: November 14, 2025
Experience Required: 1–3 years
Category: Clinical Research

About the Role

Illingworth Research Group, a global leader in patient-focused clinical services and part of the Syneos Health network, is hiring a Clinical Research Coordinator II (CRC II) for its Dallas and Euless, Texas operations. The role involves hybrid on-site and remote responsibilities across multiple therapeutic areas and study phases. The CRC II will coordinate clinical trial activities in accordance with GCP, ICH guidelines, SOPs, and regulatory requirements.

This position is ideal for professionals with hands-on experience in clinical research coordination and a strong understanding of protocol-driven operations.


Key Responsibilities

1. Clinical Research Planning & Study Start-Up

  • Review study protocols, ICFs, IBs, and related documents for accuracy and feasibility.

  • Prepare and maintain the Investigator Site File and Trial Master File (TMF).

  • Participate in timeline development, start-up discussions, SIVs, and investigator meetings.

  • Lead study start-up activities including logistics planning, team training, preparation of source documents, CRFs, and lab workbooks.

  • Coordinate safety assessment requirements, QC plans, monitoring strategies, pharmacy/dispensing needs, and other operational components.

  • Ensure all regulatory and contractual documents are complete before study initiation.

  • Support the Principal Investigator with delegation logs, scheduling, visit calendars, and monitor visit coordination.

  • Assist in participant recruitment, advertising, and screening.

2. Clinical Conduct & Data Management

  • Conduct all study procedures in compliance with GCP and relevant regulations.

  • Manage multiple trials simultaneously while ensuring participant safety.

  • Perform screening coordination, informed consent assistance, data entry, CRF completion, and timely submissions.

  • Support audits, monitoring visits, and data quality checks.

  • Develop rapport with patients and study teams to prevent protocol deviations.

  • Coordinate clinic activities including admission, dosing, randomization, follow-up, and discharge.

  • Oversee drug administration and ensure adherence to protocol and SOPs.

  • Maintain study logs, track AEs and SAEs, and manage QC findings.

3. Close-Out Activities

  • Resolve monitor findings and QC issues.

  • Finalize CRFs, study logs, deviation reports, and documentation for archiving.

  • Oversee return of study materials, completion of IRB reports, and submission of close-out packages.

  • Support sponsor, QA, and regulatory audits.

4. Regulatory Compliance

  • Maintain protocol versions, informed consent updates, amendments, and renewal submissions.

  • Report adverse events and ensure proper regulatory documentation.

  • Maintain accurate and complete study files.

5. Additional Expectations

  • Travel up to 100% as required.

  • Maintain flexible availability (including evenings and weekends).

  • Participate in internal meetings, SOP development, and process improvement initiatives.


Required Qualifications

  • Registered Nurse (RN) or Bachelor's degree (B.Sc. or equivalent).

  • Minimum 1 year of clinical research experience; 2+ years preferred.

  • Strong understanding of ICH-GCP, privacy regulations, and clinical research guidelines.

  • Experience with clinical trial coordination, documentation, and EDC systems.

  • Skills in problem-solving, planning, time management, and multi-tasking.

  • Strong interpersonal and communication abilities.

  • Experience in SOP writing and quality-driven study processes.

  • Proficiency in MS Office (Word, Excel, PowerPoint).

Preferred: Clinical Research certification.


Compensation & Benefits

Salary Range: USD 67,700 – 115,100
(Actual compensation depends on experience, skills, and overall qualifications.)

Benefits may include:

  • Health, Dental, and Vision insurance

  • 401(k) with company match

  • Employee Stock Purchase Plan

  • Car allowance or company car (role-dependent)

  • Bonus eligibility (individual and company performance)

  • Flexible paid time off (PTO) and sick leave

  • Work-life balance support programs


About the Company

Illingworth Research Group, operating across 45+ countries, brings clinical research directly to patients through innovative home-based and site-based solutions. As part of Syneos Health, the organization focuses on advancing clinical operations while improving patient experience and trial efficiency.


Summary

This role involves coordinating and co-leading clinical research operations across multiple studies while ensuring compliance with protocols, SOPs, and regulations. Ideal for professionals seeking career growth in global clinical research settings.