Clinical Research Associate Jobs in United States

The Clinical Research Coordinator / Clinical Project Associate supports clinical trials by managing study data, drug logistics, and site documentation. They coordinate meetings, maintain supplies, and assist in quality assurance under supervision.

Clinical Research team at Cook Medical leads the oversight of vendor CRAs and monitoring activities for medical device studies. The role mentors and trains vendor staff, ensures compliance with FDA, ISO-14155 and study protocols, and drives process improvements in monitoring strategy.

IQVIA Early Clinical Development team drives Phase 1 trials across diverse therapeutics. The Senior CRA monitors sites, ensures GCP compliance, tracks enrollment, manages TMF/ISF, and collaborates with cross‑functional teams in Durham, NC, onsite.

The Pulmonary Research Program at the Cedars-Sinai Women's Guild Lung Institute aims to understand lung disease mechanisms and translate findings to improve patient health. The Clinical Research Associate I supports noncomplex research studies by collecting data, scheduling participants, assisting with IRB submissions, and ensuring regulatory compliance.

Neurology Clinical Trials Team at Georgetown University Medical Center conducts cutting‑edge research on neuroimmunology and neuromuscular disorders. The Clinical Research Associate coordinates seven active trials, schedules patient visits, ensures regulatory compliance, enters data into OnCore/CTMS, and reports adverse events while serving as the primary patient liaison.

Clinical Research team at CTTX Health focuses on advancing innovative neuroscience therapies through rigorous clinical trials. The Clinical Research Associate conducts site initiation, monitoring, and close-out visits, verifies study data, and collaborates with site staff to resolve challenges and ensure protocol compliance.

Clinical Research Associate role at Integrated Resources, Inc. involves leading 3-4 clinical studies, ensuring data integrity, and coordinating with cross‑functional teams. Candidates should have academic CRO experience, proficiency in data management, CRF design, and familiarity with FDA regulations and EDC systems.

Clinical Research Associate role at Integrated Resources, Inc. supports clinical study operations, ensuring adherence to protocols and timelines. The CRA works closely with Clinical Project Managers, assisting in document preparation, vendor coordination, and monitoring report review.

The Clinical Research Associate will oversee site monitoring and operational support across multiple domestic and international clinical trials. Reporting to the Associate Director of Clinical Operations, the role ensures adherence to SOPs, GCP, and regulatory requirements.

The Senior Clinical Research Associate at Paragonix Technologies, Inc. reports to the VP Scientific and Medical Affairs and oversees prospective randomized clinical studies across solid organ platforms. Day-to-day responsibilities include providing data coordination and management, managing investigative site activity for multiple protocols, coordinating budgets and invoicing, creating and implementing subject enrollment strategies, designing CRFs and eCRFs, and supporting reporting to clinicalt

Corcept Therapeutics’ Clinical Research & Development team drives the science of cortisol modulation to treat hypercortisolism and oncology. The Senior Clinical Research Associate independently manages small‑to‑medium studies, ensuring GCP, SOP, and protocol compliance while coordinating vendors, sites, and CROs.

IQVIA’s Clinical Research team drives site monitoring and data integrity for clinical trials. The Associate conducts GCP‑compliant site visits, manages recruitment plans, and ensures accurate CRF submission.

Structure Therapeutics is a biotech company focused on developing small molecule medicines using advanced computational and structural biology techniques. The Senior Clinical Research Associate will independently manage all clinical aspects of small to medium-sized studies, ensuring compliance with GCP, SOPs, and study protocols.

The In-House Clinical Research Associate at Ocugen supports the planning, execution, and closeout of clinical studies to ensure quality, timelines, and regulatory compliance. Day-to-day work includes study start-up and maintenance, TMF/eTMF document control and QC, CTMS data tracking, vendor and site coordination, and supporting CRAs and CTMs with operational and inspection-readiness tasks.

City of Hope's Clinical Research Associate II (CRA II) manages multiple research protocols to ensure efficiency and regulatory compliance, attending clinic as needed. Day-to-day duties include protocol management, maintaining accurate documentation, compiling and submitting data, monitoring study requirements, recruiting patients, training new staff, and collecting specimens.

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 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.

Worldwide Clinical Trials is a global, midsize CRO on a mission to improve lives by taking pioneering, creative approaches to clinical research. As a Clinical Research Associate, you will support clinical trial operations and contribute to the company's goal of changing how the world experiences CROs.

The Clinical Research Associate (CRA) role sits within Resmed’s Medical Affairs team, collaborating with Sleep, Respiratory Care, SaaS, ResMed Healthcare, and Asia Growth Markets to align clinical research and market access projects with strategic priorities while maintaining global regulatory compliance. Day-to-day, the CRA supports planning, start-up, execution, monitoring, and closeout of single- and multi-site clinical studies, including site coordination, EDC monitoring and data review, stu

Clinical Research Associate role at Integrated Resources, Inc. supports day‑to‑day clinical study operations under the Clinical Project Manager. The CRA assists in authoring study documents, oversees CRO investigator background checks, manages vendor shipments, and ensures essential documents for investigational medicine release.