In this pivotal role, you will serve as a Clinical Information Specialist on a team developing specialized clinical initiatives and programs, impacting long-term goals and objectives that support the remarkable vision of Ontada. Key Responsibilities include implementing content and data according to standard policy for medication management (commercial and investigational), clinical laboratory and radiology terminology, oncologic diagnosis coding, and clinical orders. You will create and maintain standard of care clinical oncology treatments to support Ontada Technology solutions, develop and implement general rules/logic for a variety of oncology-focused guidelines, act as content release coordinator for content releases, monitor and process requests via multiple ticketing systems, process and provide access to customers for content access, support system integrations, set up data analysis processes, and provide clinical technical support. Minimum requirements include a degree or equivalent and typically 4+ years of relevant experience. Critical skills include 4+ years of experience in clinical/healthcare field, clinical and/or pharmacy experience, familiarity with terminology such as ICD-10, CPT, SNOMED, LOINC, HCPCS, and HL7, understanding of Clinical Information Systems for documentation of patient care delivery, collaboration with customers and other departments to support company initiatives, understanding and capability to write operational and functional requirements, and knowledge of computer system software components such as Microsoft Office Suite and Windows. Additional skills include critical thinking, attention to detail, proven communication skills, excellence in customer service, ability to maintain organized documentation, ability to think and act independently while adhering to guidelines, and preferred health field related certifications or degrees (CPC, CPhT, MLT, etc.). Candidates must be authorized to work in the USA; sponsorship is not available for this role.
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