Clinical Research Coordinator 247118

Medix™; Tyler (TX); On-site; USD 38,572 - 48,216; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Disability insurance

Job summary

A leading healthcare provider in Tyler, TX, is seeking a Clinical Research Coordinator to support clinical trial operations. This hands-on role involves engaging with patients, managing data, and ensuring compliance with trial protocols. The ideal candidate possesses strong clinical research expertise and the ability to work independently in a fast-paced environment. This full-time position offers competitive pay and significant opportunities for professional growth.

Qualifications

• Hands-on experience as a Clinical Research Coordinator.
• Strong understanding of clinical trial protocols and processes.
• Proven ability to work independently in a fast-paced environment.

Responsibilities

• Engage directly with patients for clinical trial activities.
• Screen and enroll participants according to protocol-defined criteria.
• Collect, document, and manage clinical trial data accurately.

Skills

Patient recruitment

Clinical trial protocols understanding

Documentation and data management

Independent work

Strong communication skills

Job description

This range is provided by Medix™. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$28.00/hr - $35.00/hr

Direct message the job poster from Medix™

Schedule: Monday – Thursday, 8:00 AM – 5:00 PM; occasional Fridays. Flexibility required as the study pipeline grows.

Primary Site: 2737 S. Broadway, Tyler, TX 75701 (occasional travel to nearby hospital)

Overview:

We are seeking a highly motivated Clinical Research Coordinator (CRC) with strong patient-facing experience to support clinical trial operations at a busy research site in Tyler, TX. This is a hands-on role requiring initiative, clinical research expertise, and the ability to work independently alongside a fast-paced Principal Investigator.

Key Responsibilities:

• Engage directly with patients for clinical trial activities
• Screen and enroll participants according to protocol-defined inclusion/exclusion criteria
• Thoroughly review and interpret clinical trial protocols
• Collect, document, and manage clinical trial data with a high level of accuracy
• Conduct registry trial assessments, including review and documentation of patient pain scales
• Collaborate with the Principal Investigator to ensure studies remain on track

Preferred Experience:

• Previous experience in patient recruitment
• Background in orthopedic or device trials
• Familiarity with device/implant studies for back and knee
• Experience with registry trials involving long-term follow-up
• Back and knee implant/device trials
• Ongoing registry studies requiring annual patient visits and assessments
• Restorative and knee-focused clinical trials

Required Qualifications:

• Hands-on experience as a Clinical Research Coordinator
• Strong understanding of clinical trial protocols and processes
• Proven ability to work independently and take initiative
• Comfortable in a fast-paced environment with minimal oversight
• Excellent documentation and data management skills

Ideal Candidate Attributes:

• Independent, confident, and proactive
• Quick-thinking and fast learner
• Strong communication and organizational skills
• Capable of managing a dynamic workload with minimal supervision

Seniority level

Associate

Employment type

Full-time

Job function

Research

Industries

Hospitals and Health Care

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

Disability insurance

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