Clinical Research Associate Jobs in Colorado, 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.

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.

Fortrea's FSP team is seeking a Clinical Research Associate 2 for the West Region to deliver high-standard clinical trial monitoring and participant care across the western United States. Day-to-day work includes full-cycle site monitoring (routine and close-out visits, pre-study/initiation visits, study file maintenance), CRF review and query resolution, SAE reporting, registry management, and acting as a local project coordinator or client contact.

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.

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.

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.

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).

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.

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.

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 FSP team at Covance is seeking a Sr. CRA 2 to provide high-standard clinical trial care and respond to emergency situations based on clinical research standards. Day-to-day responsibilities include all aspects of study site monitoring, including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaising with vendors, and other duties as assigned.

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.

Vail Health seeks a Clinical Research Coordinator to manage clinical trials within its grant-funded research program, ensuring human subject protection, data accuracy, and regulatory compliance. Day-to-day duties include managing trial documentation, coordinating patient recruitment and treatment scheduling, maintaining case report forms and regulatory files, and collaborating with clinical staff and the Principal Investigator.

Clinical Research team at CenExel conducts Phase I-IV trials across specialties like Psychiatry and Neurology. The Registered Nurse oversees daily study activities, monitors participants, documents protocols, and liaises with sponsors while ensuring safety and compliance.

Division of Pulmonary, Allergy, and Critical Care Medicine at the University of Colorado seeks a Clinical Research Coordinator to support the Asthma Research Program. The role conducts clinical visits, manages participant recruitment, data, and regulatory compliance for industry and grant‑funded studies.

CenExel RMCR in Englewood, CO is seeking a Clinical Research RN, PRN (Night Shift) to oversee daily clinical study activities across Phase I–IV trials. The role serves as a liaison between the investigative site and the Sponsor, accurately and ethically documenting all clinical research information.

The Department of Emergency Medicine and the ATLAS (Airways, Trauma, Lung Injury and Sepsis) Lab Research Program at the University of Colorado Anschutz Medical Campus seeks an Intermediate or Senior Research Services Clinical Sciences Professional. The role coordinates observational and interventional clinical trials for critically ill and injured patients in the Emergency Department and ICUs, handling screening, consenting, enrollment, data collection, and regulatory compliance.

The Neurovascular Clinical Research team at Medtronic supports global clinical development of therapies for stroke and other neurovascular conditions. The Senior Clinical Research Specialist authors and leads clinical, scientific, and regulatory documentation, develops evidence strategies, and partners with cross-functional stakeholders to advance study start-up, execution, publication planning, and regulatory submissions.