New · posted Nov 1
IQVIA · Pharmaceuticals
Clinical Research Coordinator
- Brownsville, TX
- On-site
- Part-time
- Associate & Specialist
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.
Clinical Research Coordinator - Brownsville, TX
Work Set-Up: On-site Schedule Weekly Hours: 16 hours/week
What you need
- Bachelor’s degree preferred or equivalent combination of education and relevant experience.
- Minimum 1+ years of relevant work experience in clinical research.
- Working knowledge of clinical trials, GCP principles, and medical terminology.
- Experience conducting patient study visits and participant-facing clinical research activities.
- Demonstrated ability to recruit and screen patients according to study eligibility criteria.
- Proficiency with EDC systems, including accurate data entry, query resolution, and data management processes.
- Strong attention to detail and ability to establish effective working relationships.
Please note: This position is not eligible for sponsorship.
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 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.
What you'll do
- Perform a variety of clinical procedures, including ECGs, sample collection, and vital signs assessments.
- Coordinate clinical research studies and maintain compliance with study protocols and Good Clinical Practice (GCP) guidelines.
- Conduct patient study visits and support participants throughout the research process, ensuring a positive study experience.
- Support study conduct by preparing study materials, setting up equipment, and planning logistical activities.
- Recruit, screen, and orient patients, evaluating eligibility based on study inclusion and exclusion criteria while ensuring their safety and well-being throughout the study.
- Collect, enter, and maintain accurate clinical data in case report forms (CRFs) and Electronic Data Capture (EDC) systems.
- Assist with EDC query management and resolution, working closely with investigators and monitors to ensure data accuracy, completeness, and quality.
- Collaborate with investigators, sponsors, and study monitors to address study-related issues and maintain high standards of data integrity.
- Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.
Pay
$72,800 – $87,360 a year
Employer provided$35.00 – $42.00 an hour · yearly at 2,080 hours (40 a week)
How this comparesWhere you'll work
Brownsville, TXOn-siteOpen in Maps (opens in a new tab)
More jobs in Brownsville, TX
From the posting
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.
Equal opportunity, accessibility and legal noticesIQVIA's statements, word for word
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
Job intelligence
The context around this role
Live data · November 1, 2026
Salary intelligence
How the pay compares
This role's midpoint is 27% below the US median for Clinical Research roles at this level.
This roleEmployer provided
Associate & Specialist roles in the US56 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $72,800 | — | $87,360 |
| All US (middle half) | $80,000 | $110,000 | $127,875 |
This role: IQVIA's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Clinical Research roles at the same level on Regulatory Jobs, November 1, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Research
The general path across 193 open Clinical Research roles on Regulatory Jobs, with the titles they carry most. Not IQVIA's own promotion track.
Career resources on Clinical Research
Skills DNA
What this role leans on
How many of the posting's 22 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct10
- GMP and compliance3
- Documentation and SOPs3
- Investigations and CAPA3
- Data and digital systems2
- Collaboration and leadership2
- Lab testing and methods1
- Validation and qualification1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
IQVIA on Regulatory Jobs
- 83
- Open roles
- 59
- Distinct roles
- 26
- Locations
By discipline
- Clinical72 87%
- Regulatory7 8%
- Quality4 5%
By level
- Associate & Specialist43 52%
- Manager15 18%
- Senior & Principal15 18%
More roles at IQVIA
- View role
Clinical Research Coordinator
Bountiful, UTAssociate & SpecialistPharmaceuticals$37K–$91K
- View role
Clinical Research Associate 2
Durham, NCAssociate & SpecialistPharmaceuticals$75K–$198K
- View role
(Senior) Clinical Research Associate
Durham, NCAssociate & SpecialistPharmaceuticals$90K–$175K
- View role
Clinical Research Associate II
Durham, NCAssociate & SpecialistPharmaceuticals$75K–$198K
Similar Clinical Research roles elsewhere
- View role
FSP CRA I / CRA II - U.S. South Central Region - Multiple Therapeutic Areas
Thermo Fisher ScientificRemote, TX, AR, NM, OK, LAAssociate & SpecialistPharmaceuticalsSalary not listed
- View role
FSP CRA I or II
Thermo Fisher ScientificRemote, TXAssociate & SpecialistPharmaceuticalsSalary not listed
- View role
Clinical Research Associate
ICONSan Antonio, TX +1 moreAssociate & SpecialistPharmaceuticalsSalary not listed
- View role
Clinical Research Associate
ICONTexas · HybridAssociate & SpecialistPharmaceuticalsSalary not listed
Clinical Research Coordinator at IQVIA
Open until filled. $73K–$87K a year, employer provided.