McKesson · 7 hours ago
Clinical Research Coordinator
Las Vegas, NV
Full-time
Onsite
Entry, Mid Level
1+ years expMcKesson, through its subsidiary Sarah Cannon Research Institute (SCRI), is dedicated to advancing oncology treatments and improving outcomes for cancer patients. The Clinical Research Coordinator will oversee the clinical operations of the blood cancer research program, including patient enrollment, data management, and regulatory compliance.
BiopharmaBiotechnologyHealth CareInformation TechnologyPharmaceutical
Responsibilities
You will support enrolling patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements
You will review the study design and inclusion/exclusion criteria with physicians and patients
You will ensure the protection of study patients by verifying informed consent procedures and adhering to protocol requirements
You will collect, complete, and enter data into study specific case report forms (CRFs) or electronic data capture systems within study required timelines
You will ensure the integrity of the data submitted on case report forms or other data collection tools by careful source document review and monitoring data for missing or implausible data
You will create study specific tools for source documentation when not provided by sponsor
You will generate and track drug shipments, lab kits, and other supplies
You will be responsible for accurate and complete documentation of protocol requirements according to site work instructions and standard operating procedures (SOPs)
You will track and report adverse events, serious adverse events, protocol waivers, and deviations
You will maintain accurate and complete records, including regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, screening and enrollment logs, and study communications
You will coordinate regular site research meetings
You will attend study-specific on-site meetings/visits, investigator meetings, conference calls, and other coordinator meetings, as required and you will work closely with monitors, study teams and site staff to ensure quality study data
You will communicate site status through a weekly activity report to appropriate site/management colleagues
Qualification
Required
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 the 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
Preferred
At least one year of experience managing blood cancer and/or BMT clinical trials
Research certification (ACRP or CCRP)
RN or LPN
Benefits
Comprehensive benefits to support physical, mental, and financial well-being
Competitive compensation package
Annual bonus or long-term incentive opportunities
Company
McKesson
McKesson distributes medical supplies, information technology, and care management products and services.
10001+ employees
H1B Sponsorship
McKesson has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (149)
2024 (129)
2023 (82)
2022 (142)
2021 (144)
2020 (154)
Funding
Current Stage
Public CompanyTotal Funding
unknown1994-11-18IPO
Leadership Team
Brian Tyler
CEO
Jim McAuliffe
CFO
Recent News
2026-01-12
2026-01-06
2026-01-03
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