Medix™
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 Referrals increase your chances of interviewing at Medix™ by 2x Inferred from the description for this job
Medical insurance Vision insurance 401(k) Disability insurance Get notified about new Clinical Research Coordinator jobs in Tyler, TX.
#J-18808-Ljbffr
$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 Referrals increase your chances of interviewing at Medix™ by 2x Inferred from the description for this job
Medical insurance Vision insurance 401(k) Disability insurance Get notified about new Clinical Research Coordinator jobs in Tyler, TX.
#J-18808-Ljbffr