Clinical Research Pharmacy Coordinator - 248149 (Denver)
Clinical Research Pharmacy Coordinator - 248149 (Denver)
Medix • Denver, CO, US
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Essential Duties and Responsibilities :
Maintain comprehensive and accurate patient records, including demographics, medication lists, disease states, allergies, insurance, and prescription information. Utilize pharmacy management systems to screen for drug interactions.
Process prescriptions and handle insurance billing, including troubleshooting Medicare Part B verification requirements.
Submit prior authorizations and assist patients with financial support through manufacturer or foundation programs for high-cost oral medications. Serve as a subject matter expert for staff on financial assistance and billing for oral drugs.
Provide guidance to staff regarding dispensing oral medications and navigating financial assistance programs.
Ensure cost-effective drug ordering from vendors, and receive, verify, and process drug orders. Assist with recalls and the return of expired or unused medications.
Prepare, label, and verify prescriptions in coordination with physicians or pharmacists. Obtain necessary signatures from patients or representatives, and maintain prescription documentation and daily reports.
Document all patient interactions and outcomes in the EHR, and support patient monitoring activities, including refills, adherence, and persistence.
Interact with patients regarding medication dispensing, financial assistance, and follow-up support.
Uphold infection control procedures, policies, and regulations to maintain MID safety.
Maintain central drug accountability records in compliance with regulations, including blinded studies and investigational products (IP). Oversee receiving, distribution, and destruction of IP at the Midtown site.
Support label generation, IVRS IP management portals, and scheduling of monitor and audit visits related to drug accountability. Upload and review electronic documentation for accuracy.
Collaborate with on-site pharmacy teams to ensure accurate collection of IP information and provide training and education as needed.
Serve as a resource for all temperature monitoring systems across offices, and escalate any IP or temperature monitoring issues promptly to management.
Education & Experience :
High school diploma required; associates degree in a clinical, scientific, or related field preferred.
Minimum of 3 years of experience in clinical research, regulatory affairs, or oncology-related fields preferred.
Pharmacy technician experience is a plus.
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Clinical Research Coordinator • Denver, CO, US
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