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.

Premier Research’s Global Clinical Monitoring and Site Management team builds the bridge between biotech, medtech, and specialty pharma companies and the patients who need new medicines. As a Clinical Research Associate I, you deliver quality monitoring reports, conduct site visits—remote or on‑site—ensuring data integrity and patient safety, and collaborate with the Clinical Lead to proactively resolve trial issues.

Clinical Research Associate II on the Oncology & Neurology team at Thermo Fisher Scientific. The role monitors investigator sites, ensures protocol compliance, manages data accuracy, and coordinates audit readiness across multiple states.

The Clinical Research Associate will oversee site monitoring and management to ensure compliance with study protocols, regulations, and sponsor requirements. Responsibilities include conducting site visits, tracking recruitment, evaluating site practices, and managing study documentation.

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.

Clinical Research team at Merck conducts immunology trials, ensuring protocol compliance and patient safety. The CRA manages site relationships, performs remote and onsite monitoring, and oversees regulatory documentation across multiple US locations.

Clinical Research Associate II on the PPD Development team at Thermo Fisher Scientific, driving clinical monitoring and site management for oncology and ophthalmology trials. The role conducts remote and on‑site visits, applies risk‑based monitoring, ensures protocol compliance, and collaborates with investigators to maintain audit readiness.

Clinical Research Associate, Sponsor Dedicated at IQVIA is responsible for monitoring and site management across multiple U.S. locations. The role requires performing site monitoring visits—selection, initiation, monitoring, and close‑out—according to the contracted scope of work and Good Clinical Practice (GCP).

PPD Development, LP’s Clinical Research Associate team drives global clinical trials, ensuring protocol compliance and data integrity. The role monitors investigator sites, conducts risk‑based monitoring, and manages documentation across 100+ countries.

Thermo Fisher Scientific seeks a Clinical Research Associate (Level II) to monitor clinical trials across multiple U.S. sites. The role blends on‑site and remote visits, applying risk‑based monitoring, ICH‑GCP compliance, and data accuracy checks (SDR, SDV, CRF).

Clinical Research Operations at Merck conducts cardiovascular, vaccine, and infectious disease trials. The Clinical Research Associate monitors site performance, ensures compliance with ICH/GCP, manages documentation, and supports site selection and expansion.

IQVIA Early Clinical Development builds and executes Phase 1 clinical trials across diverse therapeutics. The Senior CRA monitors sites, ensures GCP compliance, and drives enrollment and data quality.

Research Associate to support clinical research and quality improvement at Denver Health. Conducts screening, consenting, chart review, sample collection, navigation, scheduling, interviews, focus groups, outcome tracking, and data management.

We are seeking Clinical Research Associates (CRAs) with oncology monitoring experience to work remotely across California, Nevada, Idaho, New Mexico, and Colorado. The role, titled Sr CRA I / CRA 2 – FSP – Oncology, involves comprehensive site monitoring and management for clinical studies under Fortrea and sponsor SOPs.

We are seeking an experienced Oncology Clinical Research Associate (CRA) to lead and support our full-service outsourcing team. The role focuses on site monitoring, data integrity, SAE reporting, and regulatory compliance for CAR‑T trials.

Cranial & Spinal Technologies (CST) at Medtronic builds integrated surgical solutions for spine and cranial conditions. The Associate Clinical Research Specialist supports post‑market clinical trials, managing site training, data quality, and regulatory compliance across the U.S. Remote within the Upper Midwest, the role requires occasional travel to investigative sites and a valid driver’s license.

Genmab’s Clinical Biomarker Assays group seeks a Principle Research Associate to design and validate clinical exploratory assays for antibody therapies. The role focuses on cytokine and soluble analyte assays in a GCLP lab, collaborating with translational research, pathology, and data science teams.

Clinical Research Coordinator at Sarah Cannon Research Institute (SCRI) leads the operational execution of blood cancer and bone marrow transplant research programs. The role oversees patient enrollment, screening, informed consent, data capture, and regulatory documentation to ensure compliance with FDA regulations and Good Clinical Practice.

Clinical Research Coordinator at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, focuses on blood cancer and bone marrow transplant research. The role involves enrolling patients into clinical trials, reviewing study designs, ensuring informed consent, collecting and entering data into CRFs or electronic capture systems, maintaining data integrity, creating source documentation tools, tracking drug shipments and supplies, documenting protocol requirements, reporting adverse events, maintaining regulatory records, coordinating site meetings, attending investigator meetings, and communicating site status via weekly reports.

Research Scientist (Clinical Research, Traumatic Brain Injury) at GDIT’s Military Health Team will lead and assist in designing, executing, and analyzing clinical investigations for the Traumatic Brain Injury Center of Excellence (TBI CoE) at Fort Carson, Colorado. The role involves formulating experimental hypotheses, developing study protocols, coordinating with multidisciplinary teams, and preparing manuscripts for peer‑review journals.