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Clinical Research Coordinator - San Antonio, TX

Job in San Antonio, Bexar County, Texas, 78208, USA
Listing for: IQVIA LLC
Full Time, Part Time position
Listed on 2026-01-29
Job specializations:
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 35 - 42 USD Hourly USD 35.00 42.00 HOUR
Job Description & How to Apply Below
Clinical Research Coordinator - San Antonio, TX page is loaded## Clinical Research Coordinator - San Antonio, TX locations:
San Antonio, TXtime type:
Full time posted on:
Posted Todayjob requisition :
R1525366#
** Clinical Research Coordinator – San Antonio, TX**#
** Work Setup:
** On-site
*
* Schedule:

** Part-time (40 hours per week)### ###
** Shape the Future of Medicine with IQVIA!**### ###
** About IQVIA**### IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device organizations to accelerate innovation and improve patient lives. Our teams combine scientific expertise with advanced technology to transform clinical trials and healthcare delivery.### ###
** What You’ll Do*** ### Perform complex clinical procedures including ECG, spirometry, sample collection, phlebotomy, and vital signs* ### Coordinate clinical research studies while ensuring adherence to study protocols and Good Clinical Practice (GCP)* ### Prepare study materials, manage logistics, and support overall site operations* ### Recruit, pre-screen, and orient volunteers, including chart reviews, physician referrals, and community outreach* ### Communicate study details effectively to potential participants and assess patient eligibility based on inclusion/exclusion criteria* ### Collect, verify, and accurately document clinical data in case report forms (CRFs) and electronic CRFs (eCRFs)* ### Perform
** EDC entry**, ensure data accuracy, and complete
** query resolution*** ### Assist with
** study visits**, drawing on previous coordinating experience* ### Support
** lab processing**, including sample handling and documentation* ### Manage
** scheduling of appointments
** for participant visits and study timelines* ### Assist with Investigator Site File maintenance and collaborate with investigators and monitors to resolve study-related issues* ### Maintain a safe environment for volunteers in alignment with Health & Safety policies### ###
** What We’re Looking For*** ### High School Diploma or equivalent education/experience* ### Minimum 1 year of relevant clinical research experience (preferred)* ### Working knowledge of clinical trials, GCP principles, and medical terminology* ### Strong attention to detail and ability to build effective working relationships* ### Experience supporting lead CRCs with patient visits, data entry, query resolution, and prescreening referrals* ### Experience in both research and clinical settings* ###

Experience with patient recruitment and prescreening; strong communication skills to discuss study details with patients* ### Familiarity with trial activities from start-up to close-out and ability to interpret inclusion/exclusion criteria* ### Regulatory experience is a plus### ###
*
* Please Note:

*
* * This position is not eligible for sponsorship.*### ### #LI-CES #LI-DNP #LI-HCP #ONSITE### IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more atIQVIA is proud to be an equal opportunity employer.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.

We appreciate your honesty and professionalism.

The potential base pay range for this role is…
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