Clinical Research Associate Jobs in Missouri, United States

Clinical Research Associate on Georgetown University’s Medical Center team, driving infectious disease trials by monitoring patients, administering investigational therapies, and ensuring protocol compliance. Day‑to‑day duties include data capture, regulatory documentation, and cross‑functional collaboration with the Clinical Trial Office, Pharmacy, and research coordinators.

Allucent Clinical Operations team drives innovative clinical trials for small‑medium biopharma. As a Clinical Research Associate you will independently monitor investigational sites across the United States, ensure protocol compliance, and mentor junior CRAs.

Clinical Operations team at BrainChild Bio drives the execution of CAR‑T clinical trials, ensuring data integrity and patient safety. The Clinical Research Associate conducts remote and on‑site monitoring visits, performs source data review, supports data cleaning, and ensures GCP compliance across sites.

Clinical Monitoring team at WEP Clinical drives end‑to‑end oversight of clinical trial sites to ensure protocol adherence and patient safety. The Senior Clinical Research Associate conducts on‑site and remote monitoring visits, reviews study documents, manages data queries, and mentors junior CRAs while maintaining compliance with GCP and regulatory standards.

SystImmune, a biopharmaceutical company developing innovative cancer treatments, seeks a Senior Clinical Research Associate to oversee oncology clinical trials. The role involves managing study sites, ensuring data quality and patient safety through on-site and remote monitoring, and coordinating with CROs and vendors.

Novotech Clinical Research team ensures trial participants' rights and data integrity across studies. The Clinical Research Associate builds site relationships, prepares regulatory documents, monitors sites onsite or remotely, and verifies data compliance with ICH GCP and sponsor SOPs.

PSI CRO is a privately held, global Contract Research Organization founded in 1995, dedicated to advancing medical science and bringing new therapies to patients worldwide. As a Lead Clinical Research Associate, you will provide leadership, oversight, and mentorship across regional clinical trials, partnering with Project Managers, Regional Project Leads, CRAs, and cross-functional teams to ensure high-quality study execution.

PSI, a global clinical research organization founded in 1995, is hiring a Senior Clinical Research Associate to ensure the quality and compliance of medical science projects. The role involves conducting onsite monitoring visits, managing site relationships, and supervising study timelines for complex oncology trials.

The Senior Clinical Research Associate (Field-Based) at NAMSA supports the Clinical Study Manager (CSM) and Core Laboratory management, reporting to the project lead(s). The role coordinates clinical site monitoring for assigned studies, conducts on-site and remote site qualification, initiation, interim, and close-out monitoring visits, and serves as the primary point of contact for site questions on enrollment, conduct, and close-out issues.

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.

The FSP team seeks a Clinical Research Associate 2 to ensure high standards of care and protocol adherence for participants in clinical trials. This role involves comprehensive site monitoring, data integrity verification via CRF review, and Serious Adverse Event reporting across California or Colorado.

Pulse Biosciences seeks a Sr. Clinical Research Associate to support the execution of soft tissue ablation clinical trials for its CellFX® nsPFA technology. The role involves managing site start-up, monitoring patient recruitment and data quality, and ensuring regulatory compliance across U.S.-based studies.

Fortrea's FSP team is seeking a Clinical Research Associate 2 to deliver high-standard clinical trial monitoring across Ohio, Pennsylvania, or Virginia. Day-to-day, you will manage all aspects of site monitoring (routine and close-out), conduct pre-study and initiation visits, verify informed consent and protocol adherence, review CRFs and resolve queries, handle SAE reporting, and support registry management and feasibility work.

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.

FSP team seeks a Senior Clinical Research Associate II, Oncology to oversee clinical trial monitoring and site management. The role conducts site visits, ensures protocol compliance, reviews CRFs, and handles adverse event reporting while coordinating with vendors and training staff.

The FSP team seeks an Oncology Sr. Clinical Research Associate II to ensure high standards of care and protocol adherence in clinical trials. The role involves comprehensive site monitoring, data integrity verification, SAE reporting, and coordination of designated projects.

Rho is hiring a Clinical Research Associate II or Senior CRA to join its clinical monitoring team, driving project success through rigorous site management and adherence to ICH-GCP and FDA guidelines. The role involves conducting on-site and remote monitoring visits, ensuring data audit-readiness, and mentoring junior staff within a collaborative environment.

Radiation Oncology Department at Washington University School of Medicine leads cutting‑edge cancer research. The Associate Director of Clinical Research drives strategic growth of Investigator‑Initiated Trials, oversees daily operations of the Clinical Trials Office, and integrates enterprise research systems.

Clinical Monitoring team at Rho drives successful pain management trials by overseeing site monitoring and ensuring regulatory compliance. The CRA conducts 8-10 site visits per month, performs both onsite and remote monitoring, mentors junior staff, and contributes to protocol development.

Division of Behavioral Medicine and Clinical Psychology at Cincinnati Children’s Hospital Medical Center seeks a Research Associate/Full Professor to lead an independent, externally funded program focused on internalizing disorders such as anxiety, depression, and suicide. The role involves securing and managing grant funding, conducting high-impact research on health disparities in pediatric mental health, and collaborating with the Mental and Behavioral Health Institute.