Clinical Research Coordinator - Brownsville, TX
Part-timeBrownsville, TXPart-time$35–42/hrSeen 1w agoSeen in employer's feed 3 days ago
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At a glance
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Job overview
IQVIA seeks a Clinical Research Coordinator to support clinical research studies under a principal investigator’s supervision. The role includes clinical procedures, patient visits and outreach, study coordination, participant recruitment and screening, and clinical data management. The coordinator works with investigators, sponsors, and monitors to follow study protocols and Good Clinical Practice guidelines and maintain data quality and participant safety.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Brownsville, TX
Part time
R1575479
Clinical Research Coordinator - Brownsville, TX
Work Set-Up: On-site
Schedule Weekly Hours: 16 hours/week
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.
About the Role
We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.
Key Responsibilities
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Perform a variety of clinical procedures, including ECGs, sample collection, and vital signs assessments.
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Coordinate clinical research studies and maintain compliance with study protocols and Good Clinical Practice (GCP) guidelines.
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Conduct patient study visits and support participants throughout the research process, ensuring a positive study experience.
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Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
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Recruit, screen, and orient patients, evaluating eligibility based on study inclusion and exclusion criteria while ensuring their safety and well-being throughout the study.
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Collect, enter, and maintain accurate clinical data in case report forms (CRFs) and Electronic Data Capture (EDC) systems.
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Assist with EDC query management and resolution, working closely with investigators and monitors to ensure data accuracy, completeness, and quality.
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Collaborate with investigators, sponsors, and study monitors to address study-related issues and maintain high standards of data integrity.
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Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.
Qualifications
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Bachelor’s degree preferred or equivalent combination of education and relevant experience.
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Minimum 1+ years of relevant work experience in clinical research.
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Working knowledge of clinical trials, GCP principles, and medical terminology.
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Experience conducting patient study visits and participant-facing clinical research activities.
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Demonstrated ability to recruit and screen patients according to study eligibility criteria.
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Proficiency with EDC systems, including accurate data entry, query resolution, and data management processes.
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Strong attention to detail and ability to establish effective working relationships.
Please note: This position is not eligible for sponsorship.
#LI-CES #LI-DNP #LI-HCP
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 at https://jobs.iqvia.com
IQVIA 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. https://jobs.iqvia.com/eoe
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 $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
How this job compares
Set against the 607 open Clinical Research Coordinator jobs on Olive Jobs, counted November 1, 2026.
- Pay
- This posting$35–42/hr
- US median$24–35/hr173 hourly ranges
This range's midpoint, $38.50/hr, is 33% above the US median midpoint ($29/hr) — in the top quarter of Clinical Research Coordinator hourly ranges across the US.
- Openings
- Olive Jobs lists 46 open Clinical Research Coordinator jobs in Texas and 607 across the US. 2% of them nationwide are listed as remote or flexible.
- Hiring the most in Texas
- Iterative Health20 open
- Houston Methodist8 open
- Actalent5 open
- Experience
- This posting asks for at least 1 year of experience; Clinical Research Coordinator postings that state a minimum ask for 2 years at the median (397 postings).
- Education
- 195 of the 607 open Clinical Research Coordinator jobs (32%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 1, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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