Clinical Research Coordinator The Melanoma And Skin Cancer Institute Englewood, CO Job Details Full-time $26.44 - $31.54 an hour 8 hours ago Benefits Health insurance Dental insurance 401(k) Paid time off Work from home Vision insurance 401(k) matching Professional development assistance Flexible schedule Life insurance Retirement plan Qualifications Teamwork Research ethical considerations Interpersonal skills Word processing In-person customer service HIPAA Patient safety Research project coordination Bachelor's degree Medical treatment knowledge Driving Conflict management Patient interaction Typing Collaborative Institutional Training Initiative Certification (CITI) Clinical quality assurance standards Clinical confidentiality policies Patient education Time management
Full Job Description Clinical Research Coordinator Location:
701 E Hampden Ave, Englewood, CO 80113
Company:
Cutaneous Oncology Services LLC d/b/a The Melanoma And Skin Cancer Institute Job post summary Date posted: August 4th, 2026
Pay:
$55,500.00 - $65,599.00 per year Job description:
REQUIREMENTS
General High degree of planning and organizational skills Ability to work well in a team and manage conflicts and resolve problems effectively Excellent interpersonal skills with proven written, presentation and verbal competencies Strong ability to work autonomously Strong ability to multi-task and manage competing priorities while demonstrating excellent customer service behavior Ability to drive your own vehicle for work (to and from clinics) Ability to attend tumor board meetings Ability to attend research meetings Proficiency in typing and word processing Access to reliable internet Proficiency in navigating electronic systems Exhibit a positive attitude Able to lift and carry up to twenty (20) pounds unassisted Must be able to pass a criminal background check Must be able to pass a drug screening Must complete Collaborative Institutional Training Initiative (CITI) Human Subject training Complete GCP training and CTEP credentialing Coordinates assigned studies or study tasks: visits, scheduling, source, EDC, follow-up, sponsor communication Assists MSCI Investigators in the identification, recruitment, and education of patients onto MSCI research studies Serves as an educational resource to participating patients, physicians, and associate staff in cancer research Demonstrates knowledge and understanding of GCP guidelines and regulatory requirements to maintain patient safety, confidentiality, and the integrity of the clinical trial process Demonstrates behaviors that reflect quality, professionalism, teamwork and excellence Maintains patient confidentiality at all times Develops, establishes, and maintains productive relationships with MSCI staff and all sponsors and contacts to achieve essential research outcomes Collaborates closely with the MSCI Clinical Research departments to ensure key federal/state/local regulatory objectives are met and that ethical obligations are kept
Responsibilities:
Assist with the development and implementation of clinical trial protocols Obtain informed consent from research participants Schedule and conduct research visits Collect and document research data Maintain accurate and complete medical records Monitor research participants for adverse events Prepare regulatory documents and reports Communicate with monitors and sponsors about routine visit scheduling, queries, missing documents, and study logistics. Responsible for screening potential patients which includes obtaining HIPAA authorization, informed consent for the study, reviewing medical records to determine eligibility, communication with the investigator and patient re: additional tests to be completed. Prepare patient information for registration/randomization. Notify the investigator and patient of assigned treatment and coordinate treatment start date. Responsible for ordering and/or transporting study drug, documentation of receipt and dispensing of the study drug on the Drug Accountability Record Forms (DARFs). Responsible for calculating drug dosages per protocol requirements. Responsible for obtaining required specimens per protocol and transport of said specimens to the research office for processing and shipment. Must monitor the patient throughout the active treatment phase of the study. This includes patient visits, providing investigators and clinic staff with treatment sheets/calendars of the required treatment per protocol. Collaborate closely with the investigator and clinic staff in scheduling future appointments, explaining patient diaries and/or QOL questionnaires, reporting of adverse events, recognizing serious adverse events, and the need for dose modification. Responsible for ensuring protocol adherence by understanding, communicating, and ensuring the study parameters are ordered and carried out per protocol requirements. Closely monitor the patient's response to treatment. This is accomplished through communication with the investigator, tracking results of imaging scans as per RECIST guidelines as applicable and providing the investigator with information from the protocol explaining the appropriate response. Inform and educate the investigator and/or clinic staff regarding study drug administration requirements, including required pre-medications, order of administration, monitoring time points, and the need for infusion start/stop times. Obtain all required source documentation. Assist the clinical research team with preparing the research chart for internal audits. Assist the clinical research team in preparation for external audits. Responsible for evaluation and reporting serious adverse events and expedited reporting of such events if required (SAEs). Reporting protocol violations/deviations to appropriate stakeholders. Additional tasks and/or special projects as requested by supervisor or leadership team. Works with moderate supervision; escalates questions to PI, senior CRC, research manager, or regulatory lead.
Qualifications:
Bachelor's degree in nursing, biology, or a related field Oncology experience strongly preferred Minimum of one year of experience in clinical research Strong organizational and time management skills Excellent communication and interpersonal skills Ability to work independently and as part of a team
Benefits:
Competitive salary and benefits package Opportunity to work on cutting-edge clinical research Make a difference in the lives of others Be part of a supportive and collaborative team Education & Experience Bachelor's Degree from an accredited four (4) year college or university. One (1) year of experience working in health research. One (1) year of oncology clinical trials experience preferred.
Job Type:
Full-time Benefits:
401(k) 401(k) matching Dental insurance Flexible schedule Health insurance Life insurance Paid time off Professional development assistance Clinical Research Training Program Provided Retirement plan Vision insurance
Medical Specialty:
Oncology Schedule:
8 hour shift Day shift Monday to Friday Work from home office Ability to
Commute:
Englewood, CO 80113 (Required), Lakewood,CO 80215 (Required) Ability to
Relocate:
Englewood, CO 80113: Relocate before starting work (Required)
Work Location:
In person
Pay:
$26.44 - $31.54 per hour
Benefits:
401(k) Dental insurance Health insurance Life insurance Paid time off Retirement plan Vision insurance
