Pharmacy Technician (2854)

DM CLINICAL RESEARCH GROUPSouthfield, MI
39d

About The Position

The Pharmacy Technician will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.

Requirements

  • High School Diploma or equivalent required
  • Vaccine administration is required
  • Extreme attention to detail (strict adherence to procedures and protocols is essential)
  • Computer proficiency, especially Word, Excel, Outlook, and Google Docs.
  • Excellent communication and customer service skills.
  • Outgoing personality Well-organized with attention to detail.
  • Must be able to multitask.

Nice To Haves

  • Foreign Medical Graduate is a plus
  • Pharmacy Technician Certification a plus
  • Previous work experience as a Pharmacist or Pharmacy Technician is preferred
  • Previous work experience in clinical trials as an unblinded clinical research coordinator is preferred
  • LVN, RN, Pharmacy Technician Certification Preferred
  • FMG Preferred
  • Bilingual (Spanish) preferred but not required

Responsibilities

  • Lead Unblinded team operations
  • Compound and dispense prescribed IP as needed by Sponsor approved protocol.
  • Supervise and maintain records of all medications
  • Ensure compliance with study-specific blinding plans.
  • Provide consultative support regarding the preparation and dosing of drugs.
  • Maintain documentation of IP accountability: receipt, dispensing, return to sponsor/destruction.
  • Interpret clinic schedule and protocol into a resource that can be used to identify the date/time to compound/prepare and dispense IP for clinical trials.
  • Understand and apply all applicable site procedures.
  • Ensure receipt and proper storage of IP and bioretention samples.
  • Manage inventory, ensuring that expired items are removed from the inventory prior to expiration, and purchasing, and delivery processes for the pharmacy.
  • Review most recent pharmacy manuals, protocols and provide input on clinical and pharmacy supply needs.
  • Meet with sponsors, monitors, auditors, and regulatory authorities to review drug accountability and other study-specific information.
  • Temperature reporting.
  • Any other duties/ tasks assigned by the manager
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