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Clinical Research Coordinator

Job in Lewisville, Denton County, Texas, 75029, USA
Listing for: PRIME CLINICAL RESEARCH INC
Full Time position
Listed on 2026-01-12
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 27 USD Hourly USD 27.00 HOUR
Job Description & How to Apply Below

Pay:
Up to $27.00 per hour

Job description:

Position Overview

We are seeking a skilled and dedicated full-time clinical research coordinator to join our research team at Prime Clinical Research. The ideal candidate should have a strong background as a clinical research coordinator with expertise and certification in phlebotomy. The clinical research coordinator will play a crucial role in providing exceptional patient care, performing phlebotomy tasks, and contributing to the smooth execution of research.

This position offers an opportunity to make a meaningful impact on patients' lives and contribute to advancements in medical research. Please note the listed pay is negotiable based on experience.

Why us?
  • A great team of clinical and non-clinical staff to work with
  • Get mentored directly/mentored by an amazing Investigators and team.
What doing a great job will look like
  • Seeing an average of 6 - 10 patient's visit per 8.5hr day.
  • Maintaining turnaround times of an hour or less 80% of the time (from patient in door time to patient out the door).
  • Building a full patient panel consistently.
  • Being a good team player
  • Aligning with culture of the organization and following leadership of the Supervisor
  • Having a great attitude that is friendly and welcoming to Team members and patients

We will help you do a great job through these trainings through the Prime Clinical Research Inc’s Onboarding process.

  • How to see 6-10 patients' visit per day and leave with no source documentation and EDC tasks incomplete.
  • How to build your clinical research career through networking and coaching.
  • How to have work-life balance
  • How to get 5-star patient ratings and increase patient satisfaction
  • How to multi-task and efficiently use the different systems in clinical research
  • How to manage patient's schedule daily and efficiently.
This opportunity is perfect for the Study coordinator who:
  • Has a strong work ethic.
  • Is willing to learn the new skills required to thrive and a quick learner.
  • Is a team player
  • Is flexible
  • Is eager to teachable, correctable, coachable
Key Responsibilities:
  • Phlebotomy Expertise:
    Perform venipuncture and capillary blood collection procedures with precision and care. Ensure patient comfort and safety during blood draws while maintaining sterile techniques.

  • Patient Care:
    Greet and prepare patients for medical procedures, collect relevant medical history, and explain procedures clearly. Assist healthcare professionals in patient examinations, treatments, and minor procedures.

  • Clinical Trials Support:
    Assist in the execution of clinical trials. Follow protocols, document procedures accurately, maintain compliance with regulatory requirements, and update CTMS. Collaborate with research staff to ensure smooth trial operations.

  • Sample Handling:
    Properly label, process, and transport collected blood and other samples. Ensure accurate documentation and timely delivery of samples to the appropriate laboratory or testing facility.

  • Administrative Tasks:
    Schedule appointments, manage patient records, and update electronic health records accurately and efficiently. Assist with billing and insurance processes as needed.

  • Patient

    Education:

    Provide patients with clear instructions for at-home care, medication administration, and follow-up appointments. Address patient questions and concerns with empathy and professionalism.

  • Infection Control:
    Adhere to strict infection control protocols to minimize the risk of cross-contamination and maintain a safe healthcare environment.

  • Patient Recruitment:
    Assist in outreach to patients about clinical trials they may be qualified to participate in.

  • Qualifications:
    • 3-5 years Clinical trial experience is required.
    • High school diploma or equivalent.
    • Strongly prefer bilingual Spanish and English-speaking candidates.
    • Current Good Clinical Practice certification.
    • Certified Phlebotomy Technician (CPT) certification is required.
    • Previous experience as a clinical research coordinator, with demonstrated proficiency in phlebotomy techniques in adults and children.
    • IATA/DOT Dangerous Goods training preferred but not required.
    • Clear understanding of medical terminology and procedures.
    • Excellent communication skills, both verbal and written.
    • Strong interpersonal skills and the ability to work effectively within a multidisciplinary healthcare team.
    • Attention to detail and strong organizational skills.
    • Proficiency in using electronic health records (EHR) systems and basic office software.

    Job Type: Full-time

    Schedule:

    Monday to Friday, Weekends as needed

    Work Location:

    In person

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