Job Description
Note: The job is a remote job and is open to candidates in USA. Sarah Cannon Research Institute (SCRI) is a leading oncology research organization focused on advancing therapies for cancer patients through community-based clinical trials. As a Research Network Pharmacist, you will lead the development and maintenance of clinical trial regimen templates, review oncology clinical trial protocols, and serve as a clinical resource for electronic order sets. Responsibilities • You will develop clinical content for electronic order sets for iKnowMed (iKM) SCRI investigational drug trials. • You will serve as a clinical resource to review SCRI protocols and develop clinical content of electronic order sets for iKM. • You will compose and maintain electronic order set content per protocol specifications for all protocols prior to study opening. • You will compose and maintain electronic order sets content for all actively enrolling clinical trial protocol amendments which require a change in the original iKM regimen order set to ensure changes are made in accordance with the protocol amendment. • You will review electronic order sets for alignment with approved SCRI standardization when appropriate per clinical trial protocol guidance. • You will serve as SCRI lead for Research Operations Council (ROC) Community of Practice for Pharmacy. • You will facilitate communication among SCRI network site pharmacists to identify issues and solutions that improve the continuity of investigational drug management for SCRI clinical trials. • You will effectively communicate internally and externally with key stakeholders to SCRI for the effective building of regimen order sets. • You will facilitate rapport between the Clinical Informatics and the central SCRI department and trial sponsors related to development of accurate regimen order sets. • You will consult with other pharmacy and/or clinical personnel, to obtain information/expertise in support of the investigational drug trials and network standards, as required. • You will be available as a resource for community oncology research sites or internal stakeholders for education on trial specifics, and drug information related to investigational trial drugs. • You will conduct training sessions with SCRI staff on clinical trial iKM regimen order sets. This training includes but is not limited to: iKM regimen checklist completion, checklist submission process, and regimen review and approval. Skills • License as a Clinical Pharmacist • Knowledge and understanding of the oncology clinical research setting • At least 5 years clinical pharmacist experience in an oncology setting • At least 5 years of experience in supporting oncology clinical trials • Knowledge of and ability to effectively engage with technology/learning new technology platforms Benefits • Comprehensive benefits to support physical, mental, and financial well-being • Competitive compensation package • Annual bonus or long-term incentive opportunities Company Overview • Sarah Cannon Research Institute is one of the world’s leading oncology research organizations conducting community-based clinical trials. It was founded in 1993, and is headquartered in Nashville, Tennessee, USA, with a workforce of 501-1000 employees. Its website is Apply tot his job