Clinical Research Associate Jobs in Texas, United States

AbbVie’s Immunology team seeks a Clinical Research Associate I to advance its pipeline by ensuring excellence in clinical research and turning science into medicine. The role involves monitoring trial sites, training staff, and managing site relationships under supervision to ensure data integrity and regulatory compliance.

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

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.

Neuralink’s Clinical team pioneers brain-computer interface technology through groundbreaking human trials. As a Clinical Research Associate in Austin, you will plan, execute, and monitor these studies to ensure regulatory compliance and participant safety.

Neuralink Clinical team pioneers brain‑computer interface trials, shaping the future of neurotechnology. As a Clinical Research Associate you will design, launch, and monitor groundbreaking device studies, conduct site visits and ensure regulatory compliance.

DiaSorin's Clinical Research team advances diagnostic solutions by conducting analytical and clinical studies for regulatory submissions. The Clinical Research Associate performs hands‑on study execution, qualifies and monitors investigational sites, prepares visit reports, and supports data collection and documentation.

Merck seeks a Clinical Research Associate to manage assigned protocols and sites within Immunology, ensuring compliance with ICH/GCP and country regulations. The role involves acting as the primary site contact, performing remote and on-site monitoring, and developing new clinical research territories across designated US locations.

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.

Axsome Therapeutics is a biopharmaceutical company developing treatments for central nervous system (CNS) conditions. The Senior Clinical Research Associate (Texas Region) is a field-based role reporting to the Senior Manager of Clinical Monitoring, responsible for site management and monitoring activities across assigned programs in Texas.

Clinical Research team at Merck conducts oncology trials across the United States. The Clinical Research Associate ensures protocol compliance, manages site relationships, and performs remote and on‑site monitoring while coordinating with cross‑functional partners.

Revival Research Institute seeks a Physician Assistant to support clinical trials in McKinney, TX. The role involves conducting participant assessments, ensuring protocol compliance, and managing safety surveillance under Principal Investigator oversight. This is a full-time, on-site position.

Clinical Research Associate I – Thermo Fisher Scientific, part of the global clinical operations team that supports pharmaceutical and biotech trials. The role conducts remote and on‑site monitoring visits, ensures protocol compliance, manages documentation, and collaborates with investigative sites to maintain data integrity.

Merck seeks a Clinical Research Associate to manage site performance and compliance for assigned protocols in Immunology. The role involves monitoring clinical trials, ensuring ICH/GCP adherence, and developing new site relationships across the US. This is a fully remote position requiring significant domestic and international travel.

The FSP team seeks a Clinical Research Associate 2 to support clinical trials on the West Coast or in Texas. This role involves comprehensive site monitoring, data integrity verification, and adverse event reporting to ensure participant safety and protocol compliance.

Merck seeks a Senior Clinical Research Associate to manage ophthalmology clinical trials across multiple US states. The role involves site monitoring, compliance oversight, and mentorship while operating remotely with significant travel.

Merck seeks a Senior Clinical Research Associate to manage ophthalmology clinical trials across the US. The role ensures site compliance with ICH/GCP standards, monitors study conduct, and mentors junior staff while maintaining strong investigator relationships. This is a fully remote position requiring residence in specific states.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Clinical Research Associate II, Cardio, manages site activities, conducts study initiation visits, and ensures regulatory compliance while supporting data collection and safety reporting.

Clinical Research Associate on Merck's Oncology team, responsible for ensuring compliance and performance of clinical trial protocols across assigned sites. The role conducts site monitoring, manages regulatory documentation, and collaborates with cross‑functional teams to support study start‑up, execution, and close‑out.

Fortrea's FSP team is hiring experienced Clinical Research Associates (CRAs) specializing in Ophthalmology monitoring across major US hub locations. The role involves full-cycle study site monitoring, CRF review, SAE reporting, and ensuring participant safety and data integrity in a fast-paced, technology-driven clinical research environment.

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.