Clinical Research Coordinator

Sarah Cannon Research Institute • Denver, CO

12d • $79,000 - $9,000

About The Position

As the Clinical Research Coordinator for Blood Cancer and Bone Marrow Transplant (BMT) research, you are responsible for overall clinical operations of the facility’s blood cancer research program, including enrollment, regulatory, quality, and site operations. You support eligible participants throughout clinical trials, from recruitment and screening through enrollment, treatment, and follow-up, in accordance with protocol requirements. The role works closely with physicians, patients, monitors, study teams, and site staff to protect participants and ensure high-quality study data.

Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, is a community-based oncology research organization focused on advancing cancer treatments and improving patient outcomes. SCRI conducts clinical trials through a research network of more than 1,300 physicians at more than 200 locations in over 20 states. The company describes its Total Rewards package as including comprehensive benefits for physical, mental, and financial well-being; further benefits information is available through McKesson.

Requirements

• Associate’s degree; a bachelor’s degree is preferred.
• Knowledge of medical and research terminology.
• Knowledge of FDA Code of Federal Regulations and Good Clinical Practice (GCP).
• Knowledge of clinical research processes.
• Public presentation skills.
• Ability to manage multiple ongoing priorities and projects with a diverse team of professionals.
• At least one year of oncology experience.
• At least one year of experience in a clinical research setting.

Nice To Haves

• At least one year of oncology experience in hematology/oncology and/or transplant is preferred.
• At least one year of experience managing blood cancer and/or BMT clinical trials is preferred.
• Research certification (ACRP or CCRP) is preferred.
• RN or LPN is preferred.
• Bachelor’s degree is preferred.

Responsibilities

• Support recruitment, screening, enrollment, treatment, and follow-up of eligible clinical trial participants according to protocol requirements.
• Review study design and inclusion/exclusion criteria with physicians and patients.
• Verify informed consent procedures and adhere to protocol requirements to protect study participants.
• Collect, complete, and enter data into study-specific case report forms (CRFs) or electronic data capture systems within required timelines.
• Ensure the integrity of submitted data through careful source-document review and monitoring for missing or implausible data.
• Create study-specific source-documentation tools when they are not provided by the sponsor.
• Generate and track drug shipments, laboratory kits, and other supplies.
• Document protocol requirements accurately and completely according to site work instructions and standard operating procedures (SOPs).
• Track and report adverse events, serious adverse events, protocol waivers, and deviations.
• Maintain complete records, including regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, screening and enrollment logs, and study communications.
• Coordinate regular site research meetings.
• Attend study-specific on-site meetings and visits, investigator meetings, conference calls, and other coordinator meetings as required.
• Work with monitors, study teams, and site staff to ensure quality study data.
• Communicate site status through a weekly activity report to appropriate site and management colleagues.
• Oversee the overall clinical operations of the facility’s blood cancer research program, including enrollment, regulatory, quality, and site operations.

Benefits

• Comprehensive benefits supporting physical, mental, and financial well-being.
• Competitive compensation package; an annual bonus or long-term incentive opportunities may also be offered.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree