Pharmacy Technician-PRN

4 months ago

San Antonio, United States Evolution Research Group Full time
Job Details

Job Location
LOC004 ECT Endeavor Clinical Trials LLC - San Antonio, TX

PRN Pharm Tech

Title: Pharmacy Technician, PRN

Location: Endeavor Clinical Trials

About us:

ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with expertise in early and late-stage neuroscience drug development. With 20 wholly owned clinical sites and 4 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 400+ in-patient beds, a large and growing database of patients suffering from mental illness, neurological disorders, sleep disorders, addictions, Acute and Chronic Pain, diabetes, and other illnesses as well as normal healthy volunteers who participate in trials for the advancement of medicine. With access to over 32 million patients/subjects and 5000 + completed trials, ERG continues to grow its capabilities and expand into indications where there are tremendous unmet medical needs in the United States and globally.

Job Description:

This role assists site pharmacist prepare and dispenses investigational drugs and materials issued by the company for ongoing research studies. The candidate will be responsible for the coordination, organization, and efficient implementation of clinical data as it relates to the conduct of site's IP Pharmacy and completes all duties under the direction of the Site Pharmacist Manager. In this role you will maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Research Pharmacy technician is guided by Good Clinical Practices (GCP), International Conference on Harmonization (ICH) guidelines, Health Insurance Portability and Accountability Act (HIPAA) and company standard operating procedures and policies.

We value the spirit of collaboration in our teams and believe that to be successful, we must be a patient-centric organization. The successful candidate will be certified as a Pharmacy Technician or be an LPN with clinical research pharmacy experience. Must be knowledgeable in medical terminology and be well organized and methodical in approach.

Responsibilities:
  • Follow step-by-step procedures and/or kits for preparation, dispensing and distribution of investigational and study drug.
  • Use codes, labels, and other predefined formats for pharmacy computer entry.
  • Establish and maintain adequate and easily retrievable recordkeeping systems for protocols, study subjects, drug inventory and dispensing investigational drugs per regulatory requirements and ICH guidance requirements for handling investigational products
  • Use drug data sheets and other documents
  • Maintain standards which assure quality, proper storage and safe use of all investigational agents and related supplies.
  • Perform ordering and stocking of investigational and study agents.
  • Perform the removal and disposal of expired stock or stock from completed or terminated studies according to protocol guidelines.
  • Complete and retain paperwork.
  • Handle investigational and study drugs according to the requirements of the sponsoring agencies.
  • Prepare special formulations of investigational agents under unusual circumstances as dictated by a particular protocol.
  • Assist with appropriate monthly pharmacy audits to ensure that company policies and procedures are met. Assist in quality assurance procedures as needed.
  • Maintain a neat and clean work area.
  • Develop a well-organized work routine.
  • Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG's objectives.
Skills and Qualifications:
  • Education and experience
    • Training and/ or certification as a Pharmacy Technician
    • Knowledgeable in medical terminology
  • Requirements
    • Must have flexible availability.
    • Must have a thorough knowledge of clinical research concepts, practices, and FDA regulations and ICH Guidelines regarding drug development phases, clinical research and data management methods.
    • Excellent verbal and written communication skills

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