Clinical Research Associate Jobs in Oklahoma, 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.

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 Research Associate II at Imperative Care, a team focused on advancing stroke and vascular disease treatments. The role supports clinical operations by managing study documentation, coordinating sites, and conducting monitoring to ensure data integrity.

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.

Clinical Research Operations at Merck conducts cardiovascular, vaccine, and infectious disease trials. The Clinical Research Associate monitors site performance, ensures compliance with ICH/GCP, manages documentation, and supports site selection and expansion.

Clinical Research Associate on the Phase I team at Covance, ensuring high‑standard care for trial participants and rigorous site monitoring. The role manages all site activities, from initiation to close‑out, and handles data integrity, SAE reporting, and vendor coordination.

AbbVie’s Clinical Research Associate I team drives the execution of clinical trials across Arkansas and Texas, ensuring protocol compliance, data integrity, and patient safety. The role serves as the primary contact for investigators, conducts site evaluations, training, and monitoring, and collaborates with central monitoring to mitigate risks.

Clinical Research Associate at IQVIA Biotech partners with biotech companies to accelerate clinical development. Responsible for onsite monitoring of clinical trial sites, ensuring compliance with GCP, ICH, and sponsor protocols.

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.

The Clinical Research Associate will oversee site monitoring and management to ensure compliance with study protocols, regulations, and sponsor requirements. Responsibilities include conducting site visits, tracking recruitment, evaluating site practices, and managing study documentation.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate manages site activities for CNS and Rare Disease studies, conducts initiation visits, ensures regulatory compliance, and supports data collection remotely while traveling regionally as needed.

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.

IQVIA Early Clinical Development builds and executes Phase 1 clinical trials across diverse therapeutics. The Senior CRA monitors sites, ensures GCP compliance, and drives enrollment and data quality.

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

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.

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.

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.

Senior Clinical Research Associate II responsible for site monitoring and management of clinical studies, ensuring compliance with SOPs, regulatory guidelines, and sponsor requirements. Leads monitoring visits, manages study files, coordinates vendor interactions, oversees data integrity, and prepares trip reports.

Clinical Research Associate team at IQVIA drives high‑quality clinical trials across multiple sites. The role leads site monitoring visits, builds investigator relationships, ensures protocol compliance, and manages study progress.

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.