Clinical Research Coordinator

Sarah Cannon Research Institute • Denver, CO

11d

About The Position

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

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

Responsibilities

• Review study designs 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.
• Review source documents and monitor data for missing or implausible information to ensure the integrity of submitted data.
• Create study-specific source documentation tools when sponsors do not provide them.
• 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 and accurate 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 closely 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.

Benefits

• Comprehensive benefits supporting physical, mental, and financial well-being.
• An annual bonus or long-term incentive opportunities may be offered in addition to base pay.

What This Job Offers

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