# Clinical Research Enrollment Coordinator

**Company**: ICON Strategic Solutions
**Location**: Fort Worth, TX
**Work arrangement**: onsite
**Experience**: mid
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Fort-Worth-TX/CRC-2_JR163407-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/clinical-research-enrollment-coordinator-a84eeef1-1e7/

## Description

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

As a Clinical Research Enrollment Coordinator, you will contribute to the advancement of innovative treatments and therapies.

**Responsibilities:**

- Leading the coordination and implementation of clinical trial activities, including patient recruitment, screening, enrollment, and follow-up, ensuring compliance with protocol requirements and regulatory standards.

- Overseeing the maintenance and organization of study documentation and regulatory files, managing study binders, case report forms (CRFs), and electronic data capture (EDC) systems.

- Collecting, recording, and entering data into study databases and EDC systems, performing data query resolution and ensuring data accuracy and completeness.

- Assisting with the preparation and submission of regulatory documents and correspondence to regulatory authorities and institutional review boards (IRBs).

- Providing guidance and training to junior staff and study team members on study procedures, protocol requirements, and regulatory compliance.

**Your Profile:**

- Bachelor's degree in life sciences, healthcare, or related field; relevant experience may be considered in lieu of a degree.

- Minimum of 2 years of experience in clinical research or healthcare setting, with demonstrated proficiency in study coordination and data management.

- Strong organizational skills and attention to detail, with the ability to effectively prioritize and manage multiple tasks and responsibilities.

- Excellent communication and interpersonal skills, with the ability to interact professionally with study participants, investigators, sponsors, and colleagues.

- Proficiency in Microsoft Office suite (Word, Excel, Outlook) and experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is preferred.

**Rewards & 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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## Skills

### Required
- life sciences
- healthcare
- clinical research
- study coordination
- data management
- Microsoft Office

### Nice to have
- electronic data capture (EDC) systems
- clinical trial management systems (CTMS)

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Fort-Worth-TX/CRC-2_JR163407-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)