Clinical Trial Coordinator Jobs

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Clinical Trial Enrollment Coordinator

IRE•Fort Worth, TX
•Onsite

About The Position

The Clinical Trial Enrollment Coordinator (CRC 2) works in a sponsor-dedicated model at ICON Strategic Solutions and contributes to the development of treatments by coordinating clinical trial activities. The role is office-based in Fort Worth, Texas. Responsibilities include patient recruitment, screening, enrollment, follow-up, study documentation and data management, regulatory submissions, and supporting junior staff and study team members.

Requirements

  • Bachelor's degree in life sciences, healthcare, or a related field; relevant experience may be considered in lieu of a degree.
  • At least 2 years of experience in clinical research or a healthcare setting, with demonstrated proficiency in study coordination and data management.
  • Strong organizational skills and attention to detail, with the ability to prioritize and manage multiple tasks and responsibilities.
  • Excellent communication and interpersonal skills, including the ability to interact professionally with study participants, investigators, sponsors, and colleagues.
  • Legal right to work in the country where the role is based.

Nice To Haves

  • Proficiency in Microsoft Office, including Word, Excel, and Outlook.
  • Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).

Responsibilities

  • Lead the coordination and implementation of clinical trial activities, including patient recruitment, screening, enrollment, and follow-up, ensuring compliance with protocol requirements and regulatory standards.
  • Maintain and organize study documentation and regulatory files, including study binders, case report forms (CRFs), and electronic data capture (EDC) systems.
  • Collect, record, and enter data into study databases and EDC systems; resolve data queries and ensure data accuracy and completeness.
  • Assist with preparing and submitting regulatory documents and correspondence to regulatory authorities and institutional review boards (IRBs).
  • Provide guidance and training to junior staff and study team members on study procedures, protocol requirements, and regulatory compliance.

Benefits

  • Competitive base salary and performance-related incentives.
  • Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.
  • Retirement and pension plans.
  • Life assurance and disability coverage.
  • Employee assistance programmes and wellbeing resources.
  • Learning and development opportunities through structured training and career pathways.

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Common questions about Clinical Trial Coordinator careers and jobs.

Based on current job postings on Teal, the average Clinical Trial Coordinator salary in the US is approximately $78,000 per year, with a typical range of $41,000 to $148,000.
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