Clinical Research Assistant Jobs in Colorado
Clinical Research Assistant jobs in Colorado are concentrated in Denver, Aurora, and Boulder, where institutions like UCHealth, Children's Hospital Colorado, and the University of Colorado Anschutz Medical Campus anchor steady hiring. Demand runs from entry-level coordinators supporting Phase I trials to experienced assistants managing oncology and rare disease protocols. Colorado's growing life sciences corridor and proximity to major academic medical centers make it one of the more active markets in the Mountain West for this role. See the openings below and apply to the ones that match your experience.
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Showing 5 of 40+ Clinical Research Assistant jobs
About Us:
CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and
integrated operations optimize every step of the clinical trial process.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Compensation:$27.93-$35.00/hour (Depending on education, experience, and skillset)
Job Summary:
Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Essential Responsibilities and Duties:
- Assists with coordinating all aspects of patient involvement from study initiation until study completion.
- Organizes research information for clinical trials.
- Observes subjects and assists with data analysis and reporting.
- Schedules the collection of data.
- Documents adverse events, protocol deviations, and other unanticipated problems appropriately.
- Reports research data to maintain quality and compliance.
- Performs administrative and regulatory duties related to the study as appropriate.
- Participates in other protocol development activities.
- Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
- Educates potential participants and caregivers on protocol specific details and expectations.
- Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
- Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Education/Experience/Skills:
- High school graduate or equivalent; Bachelors Degree, preferred.
- 0-3 years of experience in the medical field.
- Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
- Strong leadership and mentorship skills.
- Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
- Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations.
- Works independently as well as functioning as part of a team.
- Must be able to effectively communicate verbally and in writing.
Working Conditions
- Indoor, Office environment.
- Shift work, depending on location.
- Essential physical requirements include sitting, typing, standing, and walking.
- Lightly active position, occasional lifting of up to 20 pounds. Rarely lift over 20 pounds.
- Reporting to work, as scheduled, is essential.
- Overnight travel may be required for training and/or investigative meetings.
CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.
About Us:
CenExel is a leading nationwide clinical research site and patient network serving the life sciences industry. Leading in CNS and early phase studies, our 18 science-led Centers of Excellence deliver the right patients, at the right time, in the right place. Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Our world-class PIs, advanced patient engagement strategies, premium data analytics, and
integrated operations optimize every step of the clinical trial process.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Compensation:$27.93-$35.00/hour (Depending on education, experience, and skillset)
Job Summary:
Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
Essential Responsibilities and Duties:
- Assists with coordinating all aspects of patient involvement from study initiation until study completion.
- Organizes research information for clinical trials.
- Observes subjects and assists with data analysis and reporting.
- Schedules the collection of data.
- Documents adverse events, protocol deviations, and other unanticipated problems appropriately.
- Reports research data to maintain quality and compliance.
- Performs administrative and regulatory duties related to the study as appropriate.
- Participates in other protocol development activities.
- Ensures site receives accurate information and supplies from sponsors (i.e.: source, protocol, scales, supplies, approvals, contacts, etc.)
- Educates potential participants and caregivers on protocol specific details and expectations.
- Performs safety and efficacy assessments per protocol (vital signs, EKGs, blood draws and other assessments as assigned).
- Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Education/Experience/Skills:
- High school graduate or equivalent; Bachelors Degree, preferred.
- 0-3 years of experience in the medical field.
- Knowledge and understanding of Federal regulations protecting human subjects in research and that govern the conduct of clinical trials.
- Strong leadership and mentorship skills.
- Developing and maintaining effective working relationships at all levels of the organization, along with those at the sponsor and vendor level.
- Crisis management and problem solving skills; ability to react calmly and effectively in emergent situations.
- Works independently as well as functioning as part of a team.
- Must be able to effectively communicate verbally and in writing.
Working Conditions
- Indoor, Office environment.
- Shift work, depending on location.
- Essential physical requirements include sitting, typing, standing, and walking.
- Lightly active position, occasional lifting of up to 20 pounds. Rarely lift over 20 pounds.
- Reporting to work, as scheduled, is essential.
- Overnight travel may be required for training and/or investigative meetings.
CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.
See All 40 Clinical Research Assistant Jobs in Colorado
Find roles in Colorado that match your experience and apply in just a few clicks.
Find JobsClinical Research Assistant Jobs by City in Colorado
Where Colorado roles are concentrated, by current openings.
Clinical Research Assistant Job Market in Colorado
A snapshot from current Colorado openings, updated as new roles post.
Who's Hiring
- University of Colorado19
- AdventHealth Porter5
- CenExel Clinical Research2
- Rocky Mountain Cancer Centers2
- Fortrea1
Top Industries Hiring
- Healthcare & Medical Services
- Education
- Biotechnology & Pharmaceuticals
What Colorado Employers Look For
The qualifications that appear most often in clinical research assistant jobs across Colorado.
- Bachelor's degree in a life sciences, health sciences, or related field required
- Familiarity with Good Clinical Practice guidelines and ICH standards expected
- Experience with electronic data capture systems such as REDCap or Medidata preferred
- Strong organizational skills for managing regulatory documents and patient records
- Ability to obtain CITI Program certification or equivalent research ethics training
- Prior clinical or research laboratory experience in an academic or hospital setting valued
Clinical Research Assistant Jobs in Colorado: Frequently Asked Questions
How do you become a clinical research assistant in Colorado?
Most clinical research assistant positions in Colorado require a bachelor's degree in biology, public health, nursing, or a related life sciences field. Colorado does not issue a state-specific license for this role, but employers at institutions like UCHealth and Children's Hospital Colorado expect candidates to complete CITI Program research ethics certification before or shortly after hire. Gaining experience through university research labs or hospital volunteer programs at Colorado's academic medical centers strengthens applications considerably.
Which companies hire clinical research assistants in Colorado?
Colorado clinical research assistant roles are posted by University of Colorado, AdventHealth Porter, and CenExel Clinical Research and others right now, based on current listings on Migrate Mate as of August 2026. The University of Colorado Anschutz Medical Campus and affiliated health systems in the Denver-Aurora corridor are particularly consistent sources of openings.
Which Colorado cities have the most clinical research assistant jobs?
Aurora, Denver, and Colorado account for the largest share of clinical research assistant openings in Colorado. Denver and Aurora lead because of the dense concentration of academic medical centers, hospital systems, and life sciences firms along the Anschutz corridor, while Boulder draws openings from its biotech and pharmaceutical research companies.
Are there remote clinical research assistant jobs in Colorado?
Yes, but they're rare. Clinical research assistants regularly work on-site to support patient interactions, specimen handling, and regulatory document management, which limits full remote options. About 28% of clinical research assistant openings tied to Colorado are remote or hybrid as of August 2026, and those positions tend to focus on data entry, regulatory submissions, or trial monitoring tasks that do not require direct patient contact.
How can I get hired as a clinical research assistant in Colorado with little or no experience?
The most realistic entry path is applying for research coordinator internships or volunteer research positions at Colorado's academic medical centers, particularly through the University of Colorado Anschutz Medical Campus and UCHealth, which regularly bring on candidates without formal research experience. Clinical roles such as medical assistant, phlebotomist, or patient care technician at these institutions also create a natural pathway into research teams. Completing CITI Program certification independently and listing relevant coursework in biostatistics or human subjects research gives applicants a clear edge.
Where can I find and apply to clinical research assistant jobs in Colorado?
You can find and apply to clinical research assistant jobs in Colorado on Migrate Mate, which lists current openings across the state. Search the listings to find roles that match your background and apply directly to the ones that fit your experience and location preferences.
See All 40 Clinical Research Assistant Jobs in Colorado
Find roles in Colorado that match your experience and apply in just a few clicks.
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