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Sarah Cannon Research Institute · 1 day ago

Clinical Research Coordinator

Las Vegas, NV

Full-time

Onsite

Entry, Mid Level

1+ years exp

Sarah Cannon Research Institute (SCRI) is a leading oncology research organization that conducts community-based clinical trials to advance cancer treatments. The Clinical Research Coordinator for Blood Cancer and Bone Marrow Transplant (BMT) research is responsible for overseeing clinical operations, including patient enrollment and data management for blood cancer research programs.

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

Clinical research processesOncology experienceFDA regulations knowledgeResearch certificationPublic presentation skillsData entrySource document reviewRecord keepingTeam management