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Clinical Research Pharmacy Coordinator - 248149 (Denver)
Clinical Research Pharmacy Coordinator - 248149 (Denver)Medix • Denver, CO, US
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Clinical Research Pharmacy Coordinator - 248149 (Denver)

Clinical Research Pharmacy Coordinator - 248149 (Denver)

Medix • Denver, CO, US
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  • [job_card.part_time]
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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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