Clinical Research Coordinator - Brownsville, TX
IQVIA•Parsippany, TX
•Onsite
About The Position
IQVIA is seeking a Clinical Research Coordinator (CRC) to support clinical research studies under the supervision of a principal investigator. The role involves hands-on clinical procedures, community outreach, patient-facing study visits, and maintaining high standards of participant care, safety, and research compliance. The position is on-site in Brownsville, Texas, and is scheduled for 16 hours per week.
Requirements
- At least 1 year 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.
Nice To Haves
- Bachelor’s degree or equivalent combination of education and relevant experience.
Responsibilities
- Perform 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.
- Prepare study materials, set up equipment, and plan logistical activities to support study conduct.
- Recruit, screen, and orient patients; assess eligibility against study inclusion and exclusion criteria while supporting participant safety and well-being.
- 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 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 data integrity.
- Advocate for patients and maintain a safe environment in accordance with Health and Safety policies.
Benefits
- Health and welfare benefits may be offered depending on the position.
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What This Job Offers
Job Type
Part-time
Career Level
Mid Level
