University of Colorado Anschutz Medical Campus
Clinical Research Coordinator - Melanoma/Derm
University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States, 80012
Job Summary
Clinical Science Professionals at all levels perform clinical research related functions which may include patient-oriented research or research conducted with human subjects. Patient-oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new technologies. Clinical Science Professionals may also assist with epidemiologic and behavioral studies and/or outcomes research and health services research.
Key Responsibilities Entry Level or CRC I
Assist with and oversee the day-to-day operations of clinical trials and studies
Independently abstracts and records all research subject data pertaining to the research protocol onto protocol-specific Case Report Forms (CRFs) and into the clinical trials database in an accurate and timely fashion
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 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 and 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)
Collaborate with other clinical research team members, investigators, and hospital staff to ensure tests and procedures required by research protocols are performed and documented (e.g., vital signs, phlebotomy, specimen processing, electrocardiograms, research drug administration, and protocol-specific tests and procedures); follow up with appropriate persons on missing or discrepant data
Meet with monitors to respond to any question of data validity and correct/revise data as appropriate; respond to queries from sponsor
Adhere to research regulatory standards
Maintain detailed records of studies including Patient Source Document Binder to ensure compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/clinical standard operating procedures and other regulatory guidelines
Assist with sponsor, data safety monitoring, and FDA audits and responses
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
Schedule, coordinate, and prepare for sponsor monitor visits and audits in collaboration with the CCTO Regulatory Affairs, Primary CRC and other research team members.
Intermediate Level or CRC II
All above responsibilities
Independently master study materials, including but not limited to 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 Level or CRC III
All above responsibilities
Assist with developing or developing protocol-specific systems and documents including process flows, training manuals, standard operating procedures (SOPs) and Case Report Forms (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
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 description is a summary only and describes the general level of work being performed, it is not intended to be all-inclusive. The duties of this position may change from time to time and/or based on business need. We reserve the right to add or delete duties and responsibilities at the discretion of the supervisor and/or hiring authority.
Work Location Hybrid – This is not a remote position. This offer is contingent upon you working full-time, hybrid, on the Anschutz Medical Campus. You may be eligible to work a hybrid schedule after six months of employment. This benefit must be approved by your supervisor. In the event of departmental workload increase or special projects, you may be asked to report full-time on site until project completion.
Why Join Us The University of Colorado Cancer Center stands at the forefront of cancer research and patient care in Colorado. As the state’s only National Cancer Institute (NCI) designated Comprehensive Cancer Center, we hold a prestigious distinction that acknowledges our exceptional contributions to the fields of research, clinical trials, prevention, and cancer control. Our guiding vision is clear: “prevent and conquer cancer. Together.” At the heart of our mission is the work to “unite our community to overcome cancer through innovation, discovery, prevention, early detection, multidisciplinary care, and education.”
Our more than 300 members, made up of renowned physicians and researchers, conduct patient-centered research to develop innovative, state-of-the-art technologies, and treatments. Crucial to this work is the nearly 300 staff members who help expand the reach of the CU Cancer Center. Our expertise across cancer types helps us provide world-class treatment for common cancers, while offering hope for many patients with difficult or aggressive cancers who have struggled to find treatment options elsewhere.
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
There are many additional perks & programs with the CU Advantage.
Qualifications Minimum Qualifications Entry Level or CRC I
Bachelor’s degree in any field (A combination of education and related technical/paraprofessional experience may be substituted for the bachelor’s degree on a year for year basis)
Intermediate Level or CRC II
Bachelor’s degree in any field (A combination of education and related technical/paraprofessional experience may be substituted for the bachelor’s degree on a year for year basis)
One (1) year of professional clinical research experience and/or professional clinical experience post Bachelor’s degree
Senior Level or CRC III
Bachelor’s degree in any field (A combination of education and related technical/paraprofessional experience may be substituted for the bachelor’s degree on a year for year basis)
Two (2) years of professional clinical research experience and professional clinical experience post Bachelor’s degree
Applicants must meet minimum qualifications at the time of application.
Clinical Research Coordinators (CRC) are not eligible for sponsorship.
Preferred Qualifications
Bachelor’s degree in science or health related field
Three (3) years of clinical research or related experience
Experience with electronic data capture systems (e.g., EMR or EHR and data management systems)
Additional certification (one of the following):
CCRC – Certified Clinical Research Coordinator
CCRP – Certified Clinical Research Professional
CCRA – Certified Clinical Research Associate
Knowledge, Skills and Abilities
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
Knowledge of basic human anatomy, physiology medical terminology
Ability to interpret and master complex research protocol information
How to Apply For full consideration, please submit the following documents:
Letter of interest describing relevant job experiences as they relate to listed job qualifications and interest in the position (only use if a cover letter is required)
Curriculum vitae / Resume
Three to five professional references, including name, address, phone number (mobile number if appropriate), and email address
Questions should be directed to: Maegan Brander; Maegan.brander@cuanschutz.edu
Screening of Applications Begins Applications will be accepted until finalists are identified, but preference will be given to complete applications received by
December 10, 2025 . Those who do not apply by this date may or may not be considered.
Anticipated Pay Range The starting salary range for this position has been established as
HIRING RANGE
Level I (Entry) $48,446
Level II (Intermediate) $52,721
Level III (Senior) $56,995
The above salary range represents the University’s good faith and reasonable estimate of the range of possible compensation at the time of posting. This position may be eligible for overtime compensation, depending on the level.
Your total compensation goes beyond the number on your paycheck. The University of Colorado provides generous leave, health plans and retirement contributions that add to your bottom line.
Total Compensation Calculator: http://www.cu.edu/node/153125
Equal Employment Opportunity Statement CU is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws governing nondiscrimination in employment. We are committed to creating a workplace where all individuals are treated with respect and dignity, and we encourage individuals from all backgrounds to apply, including protected veterans and individuals with disabilities.
ADA Statement The University will provide reasonable accommodations to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at hr.adacoordinator@cuanschutz.edu.
Background Check Statement The University of Colorado Anschutz Medical Campus is dedicated to ensuring a safe and secure environment for our faculty, staff, students and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees.
Vaccination Statement CU Anschutz strongly encourages vaccination against the COVID-19 virus and other vaccine-preventable diseases. If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively. In addition, if you work in certain research areas or perform certain safety-sensitive job duties, you must enroll in the occupational health medical surveillance program.
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Key Responsibilities Entry Level or CRC I
Assist with and oversee the day-to-day operations of clinical trials and studies
Independently abstracts and records all research subject data pertaining to the research protocol onto protocol-specific Case Report Forms (CRFs) and into the clinical trials database in an accurate and timely fashion
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 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 and 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)
Collaborate with other clinical research team members, investigators, and hospital staff to ensure tests and procedures required by research protocols are performed and documented (e.g., vital signs, phlebotomy, specimen processing, electrocardiograms, research drug administration, and protocol-specific tests and procedures); follow up with appropriate persons on missing or discrepant data
Meet with monitors to respond to any question of data validity and correct/revise data as appropriate; respond to queries from sponsor
Adhere to research regulatory standards
Maintain detailed records of studies including Patient Source Document Binder to ensure compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/clinical standard operating procedures and other regulatory guidelines
Assist with sponsor, data safety monitoring, and FDA audits and responses
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
Schedule, coordinate, and prepare for sponsor monitor visits and audits in collaboration with the CCTO Regulatory Affairs, Primary CRC and other research team members.
Intermediate Level or CRC II
All above responsibilities
Independently master study materials, including but not limited to 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 Level or CRC III
All above responsibilities
Assist with developing or developing protocol-specific systems and documents including process flows, training manuals, standard operating procedures (SOPs) and Case Report Forms (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
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 description is a summary only and describes the general level of work being performed, it is not intended to be all-inclusive. The duties of this position may change from time to time and/or based on business need. We reserve the right to add or delete duties and responsibilities at the discretion of the supervisor and/or hiring authority.
Work Location Hybrid – This is not a remote position. This offer is contingent upon you working full-time, hybrid, on the Anschutz Medical Campus. You may be eligible to work a hybrid schedule after six months of employment. This benefit must be approved by your supervisor. In the event of departmental workload increase or special projects, you may be asked to report full-time on site until project completion.
Why Join Us The University of Colorado Cancer Center stands at the forefront of cancer research and patient care in Colorado. As the state’s only National Cancer Institute (NCI) designated Comprehensive Cancer Center, we hold a prestigious distinction that acknowledges our exceptional contributions to the fields of research, clinical trials, prevention, and cancer control. Our guiding vision is clear: “prevent and conquer cancer. Together.” At the heart of our mission is the work to “unite our community to overcome cancer through innovation, discovery, prevention, early detection, multidisciplinary care, and education.”
Our more than 300 members, made up of renowned physicians and researchers, conduct patient-centered research to develop innovative, state-of-the-art technologies, and treatments. Crucial to this work is the nearly 300 staff members who help expand the reach of the CU Cancer Center. Our expertise across cancer types helps us provide world-class treatment for common cancers, while offering hope for many patients with difficult or aggressive cancers who have struggled to find treatment options elsewhere.
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
There are many additional perks & programs with the CU Advantage.
Qualifications Minimum Qualifications Entry Level or CRC I
Bachelor’s degree in any field (A combination of education and related technical/paraprofessional experience may be substituted for the bachelor’s degree on a year for year basis)
Intermediate Level or CRC II
Bachelor’s degree in any field (A combination of education and related technical/paraprofessional experience may be substituted for the bachelor’s degree on a year for year basis)
One (1) year of professional clinical research experience and/or professional clinical experience post Bachelor’s degree
Senior Level or CRC III
Bachelor’s degree in any field (A combination of education and related technical/paraprofessional experience may be substituted for the bachelor’s degree on a year for year basis)
Two (2) years of professional clinical research experience and professional clinical experience post Bachelor’s degree
Applicants must meet minimum qualifications at the time of application.
Clinical Research Coordinators (CRC) are not eligible for sponsorship.
Preferred Qualifications
Bachelor’s degree in science or health related field
Three (3) years of clinical research or related experience
Experience with electronic data capture systems (e.g., EMR or EHR and data management systems)
Additional certification (one of the following):
CCRC – Certified Clinical Research Coordinator
CCRP – Certified Clinical Research Professional
CCRA – Certified Clinical Research Associate
Knowledge, Skills and Abilities
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
Knowledge of basic human anatomy, physiology medical terminology
Ability to interpret and master complex research protocol information
How to Apply For full consideration, please submit the following documents:
Letter of interest describing relevant job experiences as they relate to listed job qualifications and interest in the position (only use if a cover letter is required)
Curriculum vitae / Resume
Three to five professional references, including name, address, phone number (mobile number if appropriate), and email address
Questions should be directed to: Maegan Brander; Maegan.brander@cuanschutz.edu
Screening of Applications Begins Applications will be accepted until finalists are identified, but preference will be given to complete applications received by
December 10, 2025 . Those who do not apply by this date may or may not be considered.
Anticipated Pay Range The starting salary range for this position has been established as
HIRING RANGE
Level I (Entry) $48,446
Level II (Intermediate) $52,721
Level III (Senior) $56,995
The above salary range represents the University’s good faith and reasonable estimate of the range of possible compensation at the time of posting. This position may be eligible for overtime compensation, depending on the level.
Your total compensation goes beyond the number on your paycheck. The University of Colorado provides generous leave, health plans and retirement contributions that add to your bottom line.
Total Compensation Calculator: http://www.cu.edu/node/153125
Equal Employment Opportunity Statement CU is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws governing nondiscrimination in employment. We are committed to creating a workplace where all individuals are treated with respect and dignity, and we encourage individuals from all backgrounds to apply, including protected veterans and individuals with disabilities.
ADA Statement The University will provide reasonable accommodations to applicants with disabilities throughout the employment application process. To request an accommodation pursuant to the Americans with Disabilities Act, please contact the Human Resources ADA Coordinator at hr.adacoordinator@cuanschutz.edu.
Background Check Statement The University of Colorado Anschutz Medical Campus is dedicated to ensuring a safe and secure environment for our faculty, staff, students and visitors. To assist in achieving that goal, we conduct background investigations for all prospective employees.
Vaccination Statement CU Anschutz strongly encourages vaccination against the COVID-19 virus and other vaccine-preventable diseases. If you work, visit, or volunteer in healthcare facilities or clinics operated by our affiliated hospital or clinical partners or by CU Anschutz, you will be required to comply with the vaccination and medical surveillance policies of the facilities or clinics where you work, visit, or volunteer, respectively. In addition, if you work in certain research areas or perform certain safety-sensitive job duties, you must enroll in the occupational health medical surveillance program.
#J-18808-Ljbffr