Clinical Research Associate Jobs in Texas, United States

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.

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.

As a Clinical Research Associate II - Cardio within Worldwide Clinical Trials, you will manage research activities at sites participating in Worldwide's clinical research projects. You will work through all stages of the clinical study, including identifying potential sites, performing study start-up activities such as collecting regulatory documents and supporting contract and budget negotiations, training sites to collect data properly and report safety-related events, managing site activities

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.

Join a global FSP team supporting top 50 pharmaceutical companies and 750+ biotechs across 2,700 clinical trials in 100+ countries. As an FSP Clinical Research Associate (Level I or II), you will perform and coordinate clinical monitoring and site management for one specific sponsor, conducting remote or on-site visits to assess protocol and regulatory compliance, manage documentation, and ensure audit readiness.

The Associate Clinical Research Manager assists with managing various aspects of assigned clinical trials involving patient and healthy subject populations in both inpatient and outpatient settings. Additionally, the Associate Clinical Research Manager acts as liaison between senior project team members and study subjects.

The CRA II assists in the execution of clinical studies sponsored by Penumbra to assess safety and effectiveness of products. This position works with confidential patient and company data, and interfaces with a variety of internal and external stakeholders.

To be eligible for this position, you must reside in the same country where the job is located. Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Our FSP team is currently seeking experienced CRA 2s located near major hub airports across the US with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

Our FSP team is currently seeking a CRA 2 with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

Fortrea is seeking Experienced CRA 2s to lead and support its Full Service Outsourcing team across major US hub locations. In this role, you will apply clinical judgement to monitor clinical trial sites, ensure participant safety and data integrity, and respond to emergencies per clinical research standards.

Our Phase I team is currently seeking a Clinical Research Associate with 1+ years of experience. Ideal candidates would have phase I experience and reside in Texas or Mid-West (Kansas, Missouri, Nebraska, Iowa, Colorado).

IQVIA Biotech is expanding its Clinical Monitoring team and seeks CRA 2 professionals to ensure the successful execution of clinical trials for biotech sponsors. In this role, you will monitor and manage clinical sites to ensure compliance with study protocols, regulatory requirements, and sponsor expectations, directly contributing to the integrity and quality of clinical research data.

The Clinical Research Associate (CRA) is a primary point of contact at the site level for both internal and external stakeholders, responsible for overseeing the quality, integrity and compliance of clinical trial sites in accordance with the protocol, Standard Operating Procedures (SOPs), International Council for Harmonization (ICH) Guideline for Good Clinical Practice (GCP), and applicable regulatory requirements.

Our FSP team is currently seeking a CRA 2 in West, Central, or South Regions with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

The Sr. CRA II - General Medicine - East Coast or Mid-West role supports the Full Service Outsourcing team at Covance, reporting within the Fortrea Inc. organization. You will lead and support clinical trial operations by performing all aspects of study site monitoring, including routine monitoring and close-out of clinical sites, maintenance of study files, and conduct of pre-study and initiation visits.

As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' r

Fortrea is one of the largest Clinical Research Organizations in the world, operating four Early Phase Clinical Research Units across the UK and US. As a Clinical Research Technician in Dallas, TX, you will interact directly with healthy volunteer participants, read clinical research protocols, and support Phase 1 trials that establish the safety, tolerability, and pharmacokinetics of new drugs. Day-to-day work includes screening participants, obtaining informed consent, collecting medical histo

Fortrea's Early Phase Clinical Research Unit in Dallas, TX seeks a PRN Clinical Research Technician to interact directly with healthy volunteer participants and support Phase 1 trials establishing safety, tolerability, and pharmacokinetics of new drugs. Day-to-day work includes reviewing study protocols, coordinating screening procedures, obtaining informed consent, collecting medical histories, performing vitals, blood draws, and ECGs, and maintaining accurate participant records in the study d

Fortrea, a global contract research organization, is seeking a Clinical Research Technician/Phlebotomist for its Early Phase Clinical Research team in Dallas, TX. The role involves performing vital signs, phlebotomy, and ECGs on healthy volunteers while adhering to strict clinical protocols. This is an office-based position requiring overnight weekday shifts and some weekends.