Clinical Research Associate Jobs in Colorado, United States

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

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.

Clinical Research team at Merck conducts oncology trials across the US. The Clinical Research Associate manages site relationships, ensures protocol compliance, performs remote and on‑site monitoring, and collaborates with cross‑functional groups to drive study performance. Remote work, candidates must reside in listed states, travel 65‑75% of time, 2‑3 days/week on site.

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.

<p style="text-align:left"><b>Job Description</b></p><p style="text-align:inherit"></p><p><b><u>CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS</u>: ALABAMA, GEORGIA, COLORADO, MASSACHUSETTS, MICHIGAN, MARYLAND, PENNSYLVANIA</b></p><p></p><p>The role is accountable for performance and compliance for assigned protocols and sites in a country.</p><p></p><p>Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company

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.

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.

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.

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.

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.

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 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.

Join a global clinical research team that has supported the top 50 pharmaceutical companies and 750+ biotechs across 2,700 trials in 100+ countries. As an Assistant Clinical Research Associate, you will perform remote activities on assigned projects in liaison with the CRA and study Clinical Lead, providing support with site preparedness, logistical support to the monitoring process, and assisting with site management and remote monitoring tasks per SOPs and regulatory guidelines.

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.

CenExel Clinical Research Laboratory team ensures accurate lab operations supporting CNS and early phase clinical trials. The Laboratory Manager oversees daily technical functions, staff supervision, compliance with FDA/ICH/GCP, and inventory management, while coordinating sample processing and shipments.

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.

CenExel RMCR in Englewood, CO is seeking a Clinical Research Coordinator to assist with coordinating clinical trials in strict adherence to ICH, GCP, protocol, and company guidelines. Day-to-day duties include coordinating patient involvement from study initiation to completion, organizing research information, observing subjects, scheduling data collection, documenting adverse events and protocol deviations, and performing safety and efficacy assessments such as vital signs, EKGs, and blood dra

Colorado Physician Health Program (CPHP) at the University of Colorado coordinates outreach and partnership development to support community healthcare workforce across Mesa County and the Western Slope. The Clinical Research Coordinator manages the partner recruitment pipeline, schedules virtual and in‑person engagement meetings, tracks activities in REDCap and SharePoint, and provides status updates to leadership.

Clinical Research team at Panorama Eyecare conducts clinical trials to bring novel eye care treatments to patients. The Manager oversees patient care activities, recruits participants, leads research staff, ensures regulatory compliance, and negotiates study budgets.