Research Coordinator Jobs in Colorado
Research Coordinator jobs in Colorado concentrate in clinical trials, academic research, and public health, with the state's life sciences corridor and major research universities driving consistent demand from entry-level coordinators to senior clinical research associates. Denver, Aurora, and Boulder account for the largest share of openings, anchored by institutions such as UCHealth, Children's Hospital Colorado, and the University of Colorado Anschutz Medical Campus. The most in-demand specialties are oncology and cancer research, behavioral and mental health studies, and environmental or public health research. Scan the live roles below and apply to whichever ones fit.
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Showing 5 of 24+ Research Coordinator 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 24 Research Coordinator Jobs in Colorado
Find roles in Colorado that match your experience and apply in just a few clicks.
Find Research Coordinator JobsResearch Coordinator Jobs by City in Colorado
Where Colorado roles are concentrated, by current openings.
Research Coordinator Job Market in Colorado
A snapshot from current Colorado openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Healthcare & Medical Services
- Biotechnology & Pharmaceuticals
What Colorado Employers Look For
The qualifications that appear most often in research coordinator jobs across Colorado.
- Bachelor's degree in life sciences, public health, or a related field required
- Experience with IRB submissions and human subjects research protocols preferred
- Familiarity with clinical trial management systems such as REDCap or OnCore
- CITI Program certification in human subjects research or GCP training completed
- Strong documentation skills and attention to regulatory compliance and data integrity
- Ability to coordinate across research teams, sponsor representatives, and clinical staff
Research Coordinator Jobs in Colorado: Frequently Asked Questions
How do you become a research coordinator in Colorado?
Most research coordinator roles in Colorado require at minimum a bachelor's degree in a life science, public health, nursing, or related field. Colorado does not issue a state-specific research coordinator license, but most academic medical centers and clinical research organizations expect candidates to complete CITI Program training in human subjects protections and Good Clinical Practice. Earning a Certified Clinical Research Coordinator credential through ACRP or SoCRA strengthens any application and is often listed as preferred at Colorado institutions.
Which companies hire research coordinators in Colorado?
Companies currently hiring research coordinators in Colorado include University of Colorado, AdventHealth Porter, and Medpace, per current listings on Migrate Mate as of August 2026. Colorado's concentration of academic medical centers, federally funded research programs, and life sciences firms means openings appear across hospital systems, contract research organizations, and university-affiliated institutes throughout the state.
Which Colorado cities have the most research coordinator jobs?
The cities with the most research coordinator openings in Colorado are Aurora, Denver, and Basalt. Denver and Aurora dominate because of the University of Colorado Anschutz Medical Campus and the large hospital systems clustered around it, while Boulder's presence reflects its research university base and growing biotech sector that draws both academic and industry-sponsored study work.
Are there remote research coordinator jobs in Colorado?
Yes, but they're relatively limited. About 20% of research coordinator openings tied to Colorado are remote or hybrid as of August 2026, reflecting the hands-on nature of much clinical and laboratory research. The portions of the role most compatible with remote work include data entry, regulatory document management, participant follow-up by phone, and sponsor communication, while site visits and sample collection require in-person presence.
How can I get hired as a research coordinator in Colorado with little or no experience?
The most realistic entry path is applying for a research assistant or clinical research assistant role at one of Colorado's large academic medical institutions, where entry-level positions are designed to train candidates without prior study coordination experience. UCHealth and Children's Hospital Colorado both post entry-level research roles that serve as a pipeline into coordinator positions. Completing CITI training before applying, volunteering on a university-based research team at CU Boulder or CSU, or transitioning from a medical assistant or patient-facing clinical role are the lateral moves that consistently open the door in Colorado.
Where can I find and apply to research coordinator jobs in Colorado?
You can find and apply to research coordinator jobs in Colorado on Migrate Mate, which lists current Colorado openings in one place. Search the available roles, identify the ones that match your background and preferred location, and apply directly to the ones that fit.
See All 24 Research Coordinator Jobs in Colorado
Find roles in Colorado that match your experience and apply in just a few clicks.
Find Research Coordinator Jobs