• Clinical Research Coordinator II

    Urology Clinics of North Texas (Dallas, TX)


    Clinical Research Coordinator II

    Job Details

    Job Location

     

    8230 Walnut Hill Lane Ste. 700, Dallas, TX 75231 - Dallas, TX

    Description

    Clinical Research Coordinator II

     

    About the Role

     

    Urology Clinics of North Texas (UCNT) is seeking aClinical Research Coordinator II (CRC II)to join our growing clinical trials team. This is a key role for a driven, self-directed professional with a passion for high-quality clinical research and a commitment to advancing patient care.

     

    As a CRC II, you will work independently while partnering with investigators, sponsors, monitors, and cross-functional clinical teams. You'll bring your experience and critical thinking to the forefront of study execution, from protocol comprehension to proactive site operations.

     

    What You’ll Be Doing

     

    This role is designed for a confident, proactive coordinator who is ready to lead study conduct with limited oversight. Responsibilities include:

     

    + Protocol Mastery: Independently review and dissect study protocols, develop critical questions, and ensure deep understanding of objectives, procedures, and timelines.

    + Study Execution: Prepare for and lead study visits, develop source documentation, perform EDC entry, and support regulatory submissions.

    + Patient Coordination: Screen, recruit, and consent patients while ensuring ethical and thorough informed consent processes.

    + Data Quality & Reporting: Track adverse events (AE/SAE), address queries proactively, and ensure complete, high-quality data collection.

    + Stakeholder Collaboration: Regularly engage with PIs, CRAs, sponsors, and internal teams including pharmacy, lab, and regulatory units.

    + System Competence: Navigate CTMS, EDC platforms, and eRegulatory systems with ease; troubleshoot and resolve tech issues.

    + Continuous Learning: Maintain training logs, seek out educational opportunities, and stay up to date on ICH-GCP and FDA regulations.

    We’re Looking for Someone Who:

    + Has3–5 years of experienceas a Clinical Research Coordinator (oncology, urology, or therapeutic trials preferred).

    + Isself-motivated and detail-oriented, with the ability to manage multiple studies and deadlines independently.

    + Possesses a strong understanding ofGCP, FDA regulations, and IRB processes.

    + Cancommunicate effectivelywith investigators, sponsors, and multidisciplinary teams.

    + Shows initiative in learning new systems, asking strategic questions, and proactively filling knowledge gaps.

    + Is passionate about improving patient outcomes through research.

    Preferred Qualifications

    + Bachelor’s degree in life sciences or healthcare-related field

    + Certification through ACRP or SOCRA (or working toward certification)

    + Experience withelectronic data capture (EDC), CTMS, and eRegulatory systems

    + Familiarity withoncology, urology, or investigational drug studies

     

    Why Join UCNT?

     

    + Be part of a respected and research-forward urology practice

    + Collaborate with expert physicians and a dedicated clinical trials team

    + Competitive compensation, full benefits, and opportunities for career growth

    + A culture that values autonomy, innovation, and continuous development

     

    Ready to advance your career in clinical research?Apply today and join a team where your initiative, experience, and passion make a real impact.

    Qualifications

    We’re Looking for Someone Who:

    + Has3–5 years of experienceas a Clinical Research Coordinator (oncology, urology, or therapeutic trials preferred).

    + Isself-motivated and detail-oriented, with the ability to manage multiple studies and deadlines independently.

    + Possesses a strong understanding ofGCP, FDA regulations, and IRB processes.

    + Cancommunicate effectivelywith investigators, sponsors, and multidisciplinary teams.

    + Shows initiative in learning new systems, asking strategic questions, and proactively filling knowledge gaps.

    + Is passionate about improving patient outcomes through research.

    Preferred Qualifications

    + Bachelor’s degree in life sciences or healthcare-related field

    + Certification through ACRP or SOCRA (or working toward certification)

    + Experience withelectronic data capture (EDC), CTMS, and eRegulatory systems

     

    Familiarity withoncology, urology, or investigational drug studies