Pharmacy Assistant

3 weeks ago

Hialeah, United States Evolution Research Group Full time

Job DetailsJob LocationLOC003 CPMI Clinical Pharmacology Miami - Hialeah, FLDescriptionTitle: Pharmacist Assistant Location: Clinical Pharmacology of MiamiJob Description:ERG is the largest independent clinical research site services company focused on special populations and is the market leader in CNS. With 20 wholly owned clinical sites, we conduct in-patient and out-patient phase I-IV clinical research studies. Our mission is to provide the highest quality execution of clinical trials in all clinical research phases aimed at helping sponsor companies to get their life saving or life enhancing drugs to market as quickly and safely as possible. The Pharmacist Assistant is responsible for ensuring accurate preparation, dispensing, and delivery of Study drug to the Research Area. This position will be assigned, as needed, by the Medical Director to designated CPMI staff (e.g., APRN, PA, RN, Clinical Research Coordinator, and/or Director of Clinical Operations). This position will have a variable work schedule, including flexible hours and weekends.Responsibilities:Clinical: Prepare dosing sheets, with protocol number, Study drug Identification, dosing route, dosing frequency, dosage amount, or any other identifier as required per ProtocolPrepare labels for study drug with required identifiers as required per ProtocolPrepare individual unit-dosing for each study subject as required per ProtocolKnowledge of drug reactions and the synergistic effects of drugs combined with other medicationsMust be able to apply basic principles of mathematics to the calculation of problems associated with drug accountability and medication dosagesAssist CPMI management with coordinating and scheduling Study drug dosing as required per protocolKeeps apprised of all new BLS/CPR and GCP/ICH rules, regulations and proceduresAssist staff and related medical staff with study participants care as requested, to include but not limited to, lifting patients, cardiopulmonary resuscitation, bandaging and other life saving measures as directedMust be able to take pulse, blood pressure, visually observe changes in skin colorAdministrative: Maintains knowledge and understanding of SOP for data collection and study eventsUtilize standard procedures for the maintenance of positive subject identification and record appropriate collection information on proper study specific logs/flow-sheetsEnsure accurate dispensing of Study drug as required per protocolMaintains accurate account of Study drug and neat documentation records as required per protocolPerforms inventory of supplies needed and reports deficiencies to CPMI managementSupply and stock Pharmacy with needed water, cups, dispensing vials, logs, etc.Stays on duty/assigned shift until relieved by incoming staffEducational: Maintains current licensure, registration and/or certification within educational backgroundMaintains necessary CEU's for licensure, registration and/or certificationActively participates on CPMI's ongoing Quality Assurance Program, HIPAA and Compliance ProgramsKeeps apprised of all new OSHA and GCP/ICH rules and regulationsAttends all appropriate team meetings regarding study protocolsReads and understands CPMI policy and procedures manuals, SOP manual, and employee handbookAdditional Responsibilities: Complies with all CPMI Policies and Procedures, especially those regarding protocol confidentialityDemonstrates a caring, professional attitude and behavior toward study participants and staff, actively contributing to the well-being and dignity of the clinicMaintains an overall good work attitude, promoting cooperation and professionalism and interactions with other staff membersMaintains assigned work areas in a clean, safe condition, and reports any potential hazards immediatelyPerforms all other duties as properly assignedSkills and Qualifications:Education and experienceProfessional License, Registration and/or Certification in an Health Fields and at least one year of continuous experience in Clinical Research; ACLS or BLS/CPR valid certification preferred but not required;RequirementsUnderstands regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines. Knowledgeable in medical terminology Excellent communication skills (interpersonal, written, verbal) Ability to perform overnight business travel Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)Bilingual skills are preferred but not required

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