University of Colorado
Clinical Research Professional (Open Rank)
University of Colorado, Aurora, Colorado, United States, 80012
Clinical Research Professional (Open Rank)
University of Colorado Anschutz Medical Campus
Key Responsibilities
Entry Professional
Assist with and oversee the day‑to‑day operations of clinical trials and studies
Obtain study subject's medical history and current medication information, review research protocol inclusion/exclusion criteria, and confirm eligibility of subject to participate in clinical trial
Perform informed consent process or ensure that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required
Interview prospective subjects for a variety of research clinical trials; educate potential subjects on the details of the studies through phone contacts and personal interviews
Schedule subject participation in research clinical trial, coordinating availability of necessary space and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy)
Collect, code, and analyze data obtained from research in an accurate and timely manner
Adhere to research regulatory standards
Maintain detailed records of studies to ensure compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/clinical standard operating procedures and other regulatory guidelines
Participate in subject recruitment efforts, including communicating with patients expressing an interest and all pre‑screening/screening activities
Ensure that the necessary supplies and equipment for studies are in stock and in working order
Intermediate Professional
(all Entry responsibilities plus)
Independently master study materials, including protocols, informed consent forms, and all other essential study documents for assigned studies
Independently perform study related processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies
Assist team leads, supervisors and/or management with creation and implementation of processes and procedures and quality improvement initiatives
Act as a primary coordinator on multiple trials/studies
Assist and train junior team members
Senior Professional
(all Intermediate responsibilities plus)
Assist with developing or developing protocol‑specific systems and documents including process flows, training manuals, SOPs and CRFs; maintain subject‑level documentation and prepare documents, equipment and/or supplies
Assist with identifying issues related to operational efficiency and share results with leadership
Collect information to determine feasibility, recruitment and retention strategies; employ, evaluate and assist with the implementation of innovative solutions to maximize recruitment and retention
Serve as a resource and participate in study initiation and close‑out duties
This position will require occasional after‑hours and weekend work.
Work Location Hybrid
Benefits
Medical: Multiple plan options
Dental: Multiple plan options
Additional Insurance: Disability, Life, Vision
Retirement 401(a) Plan: Employer contributes 10% of your gross pay
Paid Time Off: Accruals over the year
Vacation Days: 22/year (maximum accrual 352 hours)
Sick Days: 15/year (unlimited maximum accrual)
Holiday Days: 10/year
Tuition Benefit: Employees have access to this benefit on all CU campuses
ECO Pass: Reduced rate RTD Bus and light rail service
Qualifications
Entry Professional Bachelor's degree in biology, molecular biology, chemistry, genetics or related field
Intermediate Professional
Bachelor's degree in biology, molecular biology, chemistry, genetics or related field
One (1) year professional level clinical research or related experience
Senior Professional
Bachelor's degree in biology, molecular biology, chemistry, genetics or related field
Two (2) years clinical research or related experience
A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor's degree on a year‑for‑year basis.
Preferred Qualifications
Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)
Ability to communicate effectively, both in writing and orally
Ability to establish and maintain effective working relationships with employees at all levels throughout the institution
Outstanding customer service skills
Demonstrated commitment and leadership ability to advance diversity and inclusion
Knowledge of basic human anatomy, physiology medical terminology
Ability to interpret and master complex research protocol information
How to Apply
A letter of interest describing relevant job experiences as they relate to listed job qualifications and interest in the position
Curriculum vitae / Resume
Three to five professional references, including name, address, phone number (mobile number if appropriate), and email address
To apply, visit https://cu.taleo.net/careersection/2/jobdetail.ftl?job=38440&lang=en
Application deadline: 12/23/25
Equal Employment Opportunity Statement The University of Colorado is an Equal Opportunity Employer and encourages applicants from all backgrounds. The University will provide reasonable accommodations to applicants with disabilities throughout the employment application process.
Anticipated Pay Range
Senior Professional: $56,995 - $72,498
Intermediate Professional: $52,721 - $67,061
Entry Professional: $48,446 - $61,623
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Key Responsibilities
Entry Professional
Assist with and oversee the day‑to‑day operations of clinical trials and studies
Obtain study subject's medical history and current medication information, review research protocol inclusion/exclusion criteria, and confirm eligibility of subject to participate in clinical trial
Perform informed consent process or ensure that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed as required
Interview prospective subjects for a variety of research clinical trials; educate potential subjects on the details of the studies through phone contacts and personal interviews
Schedule subject participation in research clinical trial, coordinating availability of necessary space and clinical research support (e.g., physician, nurse practitioner, laboratory, radiology, pharmacy)
Collect, code, and analyze data obtained from research in an accurate and timely manner
Adhere to research regulatory standards
Maintain detailed records of studies to ensure compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/clinical standard operating procedures and other regulatory guidelines
Participate in subject recruitment efforts, including communicating with patients expressing an interest and all pre‑screening/screening activities
Ensure that the necessary supplies and equipment for studies are in stock and in working order
Intermediate Professional
(all Entry responsibilities plus)
Independently master study materials, including protocols, informed consent forms, and all other essential study documents for assigned studies
Independently perform study related processes, procedures, and assessments as defined in study protocol and in compliance with regulating bodies
Assist team leads, supervisors and/or management with creation and implementation of processes and procedures and quality improvement initiatives
Act as a primary coordinator on multiple trials/studies
Assist and train junior team members
Senior Professional
(all Intermediate responsibilities plus)
Assist with developing or developing protocol‑specific systems and documents including process flows, training manuals, SOPs and CRFs; maintain subject‑level documentation and prepare documents, equipment and/or supplies
Assist with identifying issues related to operational efficiency and share results with leadership
Collect information to determine feasibility, recruitment and retention strategies; employ, evaluate and assist with the implementation of innovative solutions to maximize recruitment and retention
Serve as a resource and participate in study initiation and close‑out duties
This position will require occasional after‑hours and weekend work.
Work Location Hybrid
Benefits
Medical: Multiple plan options
Dental: Multiple plan options
Additional Insurance: Disability, Life, Vision
Retirement 401(a) Plan: Employer contributes 10% of your gross pay
Paid Time Off: Accruals over the year
Vacation Days: 22/year (maximum accrual 352 hours)
Sick Days: 15/year (unlimited maximum accrual)
Holiday Days: 10/year
Tuition Benefit: Employees have access to this benefit on all CU campuses
ECO Pass: Reduced rate RTD Bus and light rail service
Qualifications
Entry Professional Bachelor's degree in biology, molecular biology, chemistry, genetics or related field
Intermediate Professional
Bachelor's degree in biology, molecular biology, chemistry, genetics or related field
One (1) year professional level clinical research or related experience
Senior Professional
Bachelor's degree in biology, molecular biology, chemistry, genetics or related field
Two (2) years clinical research or related experience
A combination of education and related technical/military/paraprofessional experience may be substituted for a bachelor's degree on a year‑for‑year basis.
Preferred Qualifications
Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)
Ability to communicate effectively, both in writing and orally
Ability to establish and maintain effective working relationships with employees at all levels throughout the institution
Outstanding customer service skills
Demonstrated commitment and leadership ability to advance diversity and inclusion
Knowledge of basic human anatomy, physiology medical terminology
Ability to interpret and master complex research protocol information
How to Apply
A letter of interest describing relevant job experiences as they relate to listed job qualifications and interest in the position
Curriculum vitae / Resume
Three to five professional references, including name, address, phone number (mobile number if appropriate), and email address
To apply, visit https://cu.taleo.net/careersection/2/jobdetail.ftl?job=38440&lang=en
Application deadline: 12/23/25
Equal Employment Opportunity Statement The University of Colorado is an Equal Opportunity Employer and encourages applicants from all backgrounds. The University will provide reasonable accommodations to applicants with disabilities throughout the employment application process.
Anticipated Pay Range
Senior Professional: $56,995 - $72,498
Intermediate Professional: $52,721 - $67,061
Entry Professional: $48,446 - $61,623
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