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Alcanza Clinical Research is seeking an Investigational Product Coordinator for our Kansas City, MO location. This role prepares and dispenses study medications, ensuring compliance with GCP, ICH, HIPAA, FDA, USP 797/800, and state boards.
You will support site staff with drug distribution and staff education. You will work under the Lead Research Pharmacist and investigators, handling inventory, regulatory compliance, and patient safety, while mentoring junior staff and contributing to process
Department: Operations
Location: Kansas City Research Institute - Kansas City, MO
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Investigational Product Coordinator is responsible for preparing and dispensing study drug, providing drug-related information to subjects and staff in compliance with GCP, ICH, HIPAA, FDA, USP 797, USP 800, state Boards of Pharmacy, and company SOPs.
Under The Direction Of The Lead Research Pharmacist (or Similar) And The Principal/Sub Investigators, Conducts The Following According To Study Protocol, Company Processes & Procedures, And In Compliance With GCP, ICH, HIPPA, FDA, USP 797, USP 800, State Boards Of Pharmacy And Company SOPs
Minimum Qualifications: An associate’s degree and 1+ years’ related experience, OR an equivalent combination of education and experience, is required. Certified Pharmacy Technician (CPhT) credential is required. Bi-lingual (English / Spanish) proficiency is a plus.