Clinical Research Coordinator - Blood Cancer & BMT Trials

Sarah Cannon Research Institute; Denver (CO); Sur place; USD 79 000 - 90 000; Plein temps

Résumé du poste

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Clinical Research Coordinator for Blood Cancer and Bone Marrow Transplant (BMT) to run clinical operations, enrollment, regulatory, quality, and site operations. You will support patient enrollment on trials, review designs with physicians, and ensure informed consent compliance.

Responsibilities include data entry, source documentation, adverse event tracking, and coordination of site meetings.

Qualifications

• At least one year of oncology experience, preferably hematology/oncology and/or transplant.
• Knowledge of FDA CFR and GCP and clinical research processes.
• Public presentation skills.
• Ability to manage multiple priorities with a diverse team of professionals.
• RN or LPN is preferred.

Responsabilités

• Oversee clinical operations and enrollment for Blood Cancer/BMT trials.
• Review study design and inclusion/exclusion criteria with physicians and patients.
• Ensure informed consent procedures and protocol compliance.
• Collect, enter, and verify data in CRFs or electronic data capture systems.
• Track adverse events, serious adverse events, and protocol deviations.
• Coordinate site meetings, investigator meetings, and communications with monitors and study teams.

Connaissances

Oncology experience

GCP familiarity

Regulatory knowledge

Public presentation skills

Data management

Formation

Associate’s Degree

Bachelor’s Degree preferred

Description du poste

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Clinical Research Coordinator for Blood Cancer and Bone Marrow Transplant (BMT) to run clinical operations, enrollment, regulatory, quality, and site operations. You will support patient enrollment on trials, review designs with physicians, and ensure informed consent compliance.

Responsibilities include data entry, source documentation, adverse event tracking, and coordination of site meetings.