Clinical Research Associate Jobs in Texas, United States

Clinical Research Associate, Cell Therapy at AstraZeneca is responsible for delivering and overseeing clinical studies at allocated sites, ensuring timely and efficient execution. The role prepares, initiates, monitors, and closes sites, conducts source data verification, manages study supplies, and updates clinical systems while training and supporting site staff.

IQVIA Biotech is hiring a Clinical Research Associate (CRA) to monitor and manage clinical sites, ensuring compliance with GCP, ICH guidelines, and regulatory requirements. The role requires a minimum of 1 year of on‑site monitoring experience (CRA 2) or 6 months (CRA 1) with oncology solid tumor focus.

IQVIA’s Clinical Research team builds and monitors clinical trials to accelerate medical innovation. The Clinical Research Associate conducts site monitoring visits, manages regulatory submissions, and ensures protocol compliance across multiple study sites.

Clinical Research Associate II on the PPD Development team at Thermo Fisher Scientific, driving clinical monitoring and site management for oncology and ophthalmology trials. The role conducts remote and on‑site visits, applies risk‑based monitoring, ensures protocol compliance, and collaborates with investigators to maintain audit readiness.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas, including Oncology and Rare Diseases. The Senior Clinical Research Associate manages site activities, conducts study initiation visits, ensures regulatory compliance, and supports contract negotiations while collaborating with cross‑functional teams.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate, Rare Disease manages site activities remotely, conducts study initiation visits, ensures regulatory compliance and supports data collection.

Senior Clinical Research Associate with 2+ years on‑site monitoring experience. Conduct site monitoring, recruitment tracking, protocol training, and regulatory submissions.

Senior Clinical Research Associate at IQVIA responsible for monitoring clinical trial sites across multiple U.S. locations. Conducts site visits, ensures compliance with GCP and ICH, manages protocol training, and oversees recruitment, enrollment, and data collection.

Pediatric Research Training Program at Cook Children’s Health Care System builds evidence‑based pediatric care. The Clinical Research Intern collaborates with Principal Investigators, Research Program Coordinators, and Clinical Research Associates to maintain high‑quality data and support research projects.

Collaborates with Principal Investigators, Research Program Coordinators, and Clinical Research Associates/Coordinators as part of the Research Administration Office team. Supports data management and research administration tasks.

The Clinical Research Assistant II supports clinical research nurses and coordinators in oncology trials. Responsibilities include patient screening, data collection, regulatory compliance, and protocol adherence.

FSP Clinical Research Associate I on Thermo Fisher Scientific's Clinical Operations team, supporting global pharmaceutical and biotech trials. Conducts remote and on‑site site monitoring, ensures protocol compliance, manages documentation, and collaborates with investigational sites to maintain audit readiness.

IQVIA Biotech seeks a dedicated Clinical Research Associate (CRA) to monitor and manage clinical sites across multiple U.S. locations. The role involves conducting site visits, ensuring compliance with GCP and ICH guidelines, and maintaining regulatory documentation.

Join Thermo Fisher Scientific as a Clinical Research Associate I (CRA I) to support vaccine trials worldwide. You will conduct remote and on‑site monitoring visits, ensuring protocol compliance, data integrity, and regulatory adherence.

We are seeking an experienced Oncology Clinical Research Associate (CRA) to lead and support our full-service outsourcing team. The role focuses on site monitoring, data integrity, SAE reporting, and regulatory compliance for CAR‑T trials.

Clinical Research team at Thermo Fisher Scientific manages innovative clinical trials to advance scientific breakthroughs. The Associate Clinical Research Manager supports senior project members by overseeing documentation, data entry, EDC query resolution, and liaising with study subjects and monitors.

Clinical Research team at Thermo Fisher Scientific manages clinical trials to advance scientific innovation. The Associate Clinical Research Manager supports trial execution by coordinating with senior project members, overseeing documentation, and ensuring data quality across inpatient and outpatient settings.

Cranial & Spinal Technologies (CST) at Medtronic builds integrated surgical solutions for spine and cranial conditions. The Associate Clinical Research Specialist supports post‑market clinical trials, managing site training, data quality, and regulatory compliance across the U.S. Remote within the Upper Midwest, the role requires occasional travel to investigative sites and a valid driver’s license.

Thermo Fisher Scientific Clinical Research team advances innovative trials across patient and healthy subject populations. The Associate Clinical Research Manager supports senior project members by overseeing document accuracy, data entry, source data QC, and liaison activities with sponsors and study subjects.

Austin Retina Associates’ Clinical Research Assistant team drives retina‑specific trials, translating cutting‑edge therapies into patient care. The role supports coordinators by collecting data, performing diagnostic tests, and managing EDC systems in a fast‑paced clinical setting.