McKesson is seeking a Clinical Research Coordinator to manage the overall clinical operations of our facility’s blood cancer research program, with a focus on Blood Cancer and Bone Marrow Transplant (BMT) clinical trials. You will be responsible for enrollment, regulatory, quality, and site operations, directly supporting the fight against cancer by ensuring patients are enrolled and managed according to protocol requirements.

What You'll Do

Support enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up according to protocol requirements.
Review study design and inclusion/exclusion criteria with physicians and patients.
Ensure patient protection by verifying informed consent procedures and adhering to protocol requirements.
Collect, complete, and enter data into study-specific case report forms (CRFs) or electronic data capture systems within required timelines.
Ensure data integrity by reviewing source documents and monitoring for missing or implausible data.
Create study-specific source documentation tools when not provided by the sponsor.
Generate and track drug shipments, lab kits, and other supplies.
Maintain accurate and complete documentation according to site work instructions and standard operating procedures (SOPs).
Track and report adverse events, serious adverse events, protocol waivers, and deviations.
Maintain accurate and complete records, including regulatory documents, signed consent forms, source documentation, drug logs, and enrollment logs.
Coordinate regular site research meetings.
Attend study-specific on-site meetings/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.

What We're Looking For

An Associate’s Degree, preferably a Bachelor’s Degree.
Knowledge of medical and research terminology.
Knowledge of FDA Code of Federal Regulations and GCP.
Knowledge of clinical research processes.
Public presentation skills.
The ability to manage multiple ongoing priorities and projects with a diverse team of professionals.
At least one year of oncology experience, preferably in hematology/oncology and/or transplant.
At least one year of experience in a clinical research setting.

Nice to Have

At least one year of experience managing blood cancer and/or BMT clinical trials.
Research certification (ACRP or CCRP).
RN or LPN licensure.

Benefits & Compensation

Total Rewards package includes comprehensive benefits to support physical, mental, and financial well-being.

We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.