Sarah Cannon Research Institute · 3 hours ago

Research Site Support Pharmacist

Aurora, CO

Full-time

Remote

Senior Level

5+ years exp

Maximize your interview chances

Research Services

Insider Connection @Sarah Cannon Research Institute

Discover valuable connections within the company who might provide insights and potential referrals.
Get 3x more responses when you reach out via email instead of LinkedIn.

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 collaborate with the Research Operations Team, Clinical Informatics Team, and National Principal Investigator (NPI) as necessary.

You will compose and maintain electronic order set content per protocol specifications for all protocols prior to study opening. Ensures iKM regimen order sets are consistent with protocol requirements.

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 ensure that the iKM regimen order set is referenced with the accurate protocol version and date.

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.

Qualification

Find out how your skills align with this job's requirements. If anything seems off, you can easily click on the tags to select or unselect skills to reflect your actual expertise.

Clinical Pharmacist LicenseOncology Clinical ResearchClinical Pharmacist ExperienceOncology Clinical Trials SupportTechnology Engagement