Clinical Research Associate Jobs in Illinois, United States

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

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.

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.

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 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 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.

TFS HealthScience is a global mid-size Contract Research Organization partnering with biotechnology and pharmaceutical companies across their clinical development journey. As a Freelance Senior Clinical Research Associate (0.35 FTE) within the Clinical Development Services Ophthalmology team, you will initiate, monitor (on-site and remotely), and close out study sites, provide unmasked CRA support, manage investigational product accountability, and ensure protocol compliance and data quality.

Clinical Operations at Worldwide Clinical Trials drives multi‑therapeutic clinical studies. The Senior Clinical Research Associate manages site activities, conducts initiation visits, ensures regulatory compliance, and trains sites on data collection, all while supporting safety reporting.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate manages site activities, conducts study initiation visits, and ensures regulatory compliance while working remotely across the Central United States with regional travel.

Fortrea's FSP team is seeking a Clinical Research Associate 2 for the Central Region to deliver high-standard clinical trial monitoring and participant care across a remote territory spanning multiple states. Day-to-day, the role covers full-cycle site monitoring, pre-study and initiation visits, CRF review and query resolution, SAE reporting, and registry management, with 8-10 on-site days per month.

Clinical Research team at Merck drives cardiovascular, vaccine, and infectious disease studies. The Clinical Research Associate monitors site compliance, manages study documentation, and builds strong site relationships across the United States.

Clinical Research Associate on the Cardiovascular/Vaccine/Infectious Disease team at Merck, responsible for ensuring protocol compliance and site performance across multiple US locations. The role monitors clinical sites, manages relationships, conducts site visits, and oversees data quality and patient safety while collaborating with cross‑functional teams.

Clinical Research team at Thermo Fisher Scientific conducts multi‑site oncology, ophthalmology and neurology trials. The CRA II monitors investigator sites remotely, performs risk‑based assessments, ensures ICH‑GCP compliance, and documents findings.

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.

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.

Fortrea’s Monitoring Excellence Academy is hiring Clinical Research Associates (CRA 1) for Oncology, CAR T, or Ophthalmology trials. The role involves site monitoring, data integrity verification, SAE reporting, and supporting study site operations across Central or West coast US hubs or Montreal, Canada.

FSP team at Covance seeks Senior Clinical Research Associate 2 to lead monitoring of in‑vitro diagnostics trials across the US. The role conducts site monitoring, data verification, SAE reporting and supports site staff training while ensuring protocol compliance. Remote work from any US location with 50‑60% overnight travel required.