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Oncology Pharmacist
Halifax Health. Verify chemotherapy regimens for ordering accuracy, indication, dosing, sequencing, diluents, stability, and administration parameters .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in chemotherapy regimen verification, medication management, and aseptic compounding while ensuring compliance with safety protocols and regulatory standards. Proficient in utilizing EHR systems and managing clinical trial protocols to enhance patient care and safety.
Highest-signal resume keywords
Chemotherapy Regimen VerificationAseptic CompoundingMedication ManagementEHR Systems UtilizationClinical Trial Protocol Compliance
ATS Keywords
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Hard Skills
Chemotherapy Regimen VerificationAseptic CompoundingMedication ManagementDrug-Drug Interaction EvaluationDrug-Gene Interaction EvaluationOncology Pharmacy ProtocolsMedication ReconciliationDose Adjustment ImplementationRegulatory ComplianceIncident Review and Corrective Actions
Soft Skills
Communication with Healthcare TeamsMentoring Pharmacy TechniciansCollaboration in Care TransitionsEducation on Medication Safety
Tools & Technologies
EHR SystemsBCMASmart Pump LibrariesClinical Decision Support
Certifications & Qualifications
Florida Pharmacist License
Industry Keywords
Antineoplastic AgentsTargeted TherapiesImmunotherapiesCellular TherapiesClinical TrialsUSP RequirementsMedication SafetyQuality Compliance
About the role
Key responsibilities & impact- Verify chemotherapy regimens for ordering accuracy, indication, dosing, sequencing, diluents, stability, and administration parameters
- Assess and manage treatment toxicities, implement dose adjustments, and recommend monitoring
- Provide evidence-based recommendations for oncology therapies and clinical trial regimens
- Perform comprehensive medication management, medication reconciliation, interaction evaluation, and deprescribing when appropriate
- Oversee or perform aseptic compounding of hazardous and non-hazardous sterile preparations
- Ensure proper donning, engineering controls, closed-system transfer devices, beyond-use dating, chain-of-custody, labeling, and barcode verification
- Lead or support medication-use evaluations, incident reviews, corrective actions, protocols, order sets, and pathways
- Ensure regulatory readiness and maintain documentation and audits
- Track and report clinical interventions, outcomes, cost avoidance, and safety metrics
- Practice under collaborative practice agreements to initiate or adjust therapies, order labs, and manage supportive care
- Coordinate care transitions across infusion, inpatient, specialty pharmacy, home infusion, and community providers
- Support clinical trials and manage investigational products
- Evaluate new drugs and indications for formulary review and implementation
- Precept and mentor oncology pharmacy technicians
- Provide medication and safety education to nursing, providers, and ancillary staff
- Contribute to departmental policies, strategic initiatives, and interprofessional workgroups
- Build, validate, and maintain EHR chemotherapy plans, order sets, and clinical decision support
- Utilize BCMA and smart pump libraries and escalate issues
- Communicate with prescribers, nurses, and infusion teams to resolve order issues
- Report adverse drug events, near misses, and pharmacovigilance data
- Prioritize STAT and time-sensitive chemotherapy and supportive care orders
- Manage hazardous drug inventory, storage, and waste; coordinate shortage mitigation
- Assist with billing accuracy, NDC mapping, waste documentation, and HCPCS coding support
- Perform order verification and IV room pharmacist duties at Central Pharmacy, plus other assigned duties
Requirements
What you’ll need- Bachelor’s degree or Pharm D from an accredited College of Pharmacy
- Current valid Florida Pharmacist license
- Knowledge of chemotherapy regimen verification, antineoplastic agents, targeted therapies, immunotherapies, cellular therapies, and clinical trial regimens
- Knowledge of sterile compounding and safe handling of hazardous and non-hazardous sterile preparations per USP requirements
- Knowledge of medication safety, quality, compliance, and oncology pharmacy protocols
- Ability to practice under collaborative practice agreements (CPAs)
- Ability to use EHR chemotherapy plans, order sets, clinical decision support, BCMA, and smart pump libraries
- Ability to manage investigational products and clinical trial protocol compliance
- Ability to perform comprehensive medication management and evaluate drug–drug and drug–gene interactions