Clinical Research Coordinator

Mission

People who live with cancer – those who work to prevent it, fight it, and survive it – are at the heart of every decision we make. Bringing the most innovative medical minds together with the most passionate caregivers in their communities, we are transforming care and personalizing treatment. Through clinical excellence and cutting-edge research, SCRI is redefining cancer care around the world.

As the Clinical Research Coordinator youareresponsible foroverall clinical operations of the facility’s research program including enrollment, regulatory, quality, and site operations.

• You will supportenrolling patients onto clinical trials through recruitment, screening, enrollment, treatment, and follow-up of eligible participants according to protocol requirements.

• You will reviewthe study design and inclusion/exclusion criteria with physiciansand patients

• You will ensurethe protection of study patients by verifying informed consent procedures and adhering to protocol requirements

• You will collect, complete, and enterdata into study specific case report forms (CRFs) or electronic data capture systems within study required timelines

• You will ensurethe integrity of the datasubmittedon case report forms or other data collection tools bycareful source document review and monitoringdata for missing or implausible data

• You will createstudy specific tools for source documentation when not provided by sponsor

• You will generate and trackdrug shipments, lab kits, and other supplies

• You willberesponsible foraccurateand complete documentation of protocol requirements according to site work instructions and standard operating procedures (SOPs)

• You will track and reportadverse events, serious adverse events, protocol waivers, and deviations

• You willmaintainaccurateand complete records, including regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, screening and enrollment logs, and study communications

• You will coordinateregular site research meetings

• You will attendstudy-specific on-site meetings/visits, investigator meetings, conference calls, and other coordinator meetings, asrequiredand you will workclosely with monitors, study teams and site staff to ensure quality study data

• You will communicatesite status through a weekly activity report toappropriate site/managementcolleagues

You should have:

• AnAssociate’s Degree, preferably aBachelor’s Degree

• Knowledge of medical and research terminology

• Knowledge ofFDA Code of Federal Regulations and GCP

• Knowledge of the clinical research processes

• Public presentation skills

• The ability to manage multiple ongoing priorities and projectswith a diverse team of professionals

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As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.

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