Skip to content
Arizona Liver Health

Research Pharmacy Technician (Peoria)

Peoria, AZ; Peoria ACTUnited States
Research Pharmacy
POSTED 11 NOVVERIFIED 35M AGO
Apply Ask
Role
1 days opentrue age
Posted 11 Nov
Payin text
$23–27 / hourposted
▼ −38% vs market median $84k
$48k$140k
Market p25–p75
$55k–$140k
Arizona Liver Health p25–p75
$57k–$97kn=14
United States · n=36361 · 365d to 12 Nov
CompanyArizona Liver Health →
21open roles
Opened · 30d
+7
Closed · 30d
−7
10d of snapshots · 30d window
Market
416,853open · Other
Opened · 7d
+44,07011% of open
All other
625,341open
All tracked boards · live 12 Nov · n=416,853
GCP

About Us

Arizona Liver Health (ALH) is dedicated to driving high standards of care and advancing medical innovation through leading clinical trials, ensuring patient safety and regulatory compliance, and generating high-quality clinical data. Our network of multiphase, multitherapeutic research, standard of care, and VEN Centers sites is staffed by skilled providers, research, clinic, pharmacy, and patient outreach professionals. ALH operates state-of-the-art facilities and programs to meet the evolving needs of clinical research and overall patient treatment.

Job Summary

Arizona Liver Health/Arizona Clinical Trials is looking for qualified candidates for the Research Pharmacy Technician position in Peoria.

Title: Research Pharmacy Technician (Peoria, AZ)

Compensation: $23 - $27 per hour, depending on experience

Work Schedule: Monday-Friday, 7:00a - 4:00p (set schedule)

Essential job functions/duties

Reasonable accommodation may be made to enable individuals with disabilities to perform these essential functions.

  • Ensure adherence to protocol during study conduct and performing specific administrative and clinical procedures to assist research professionals.
  • Follow all health and safety protocols and procedures to maintain sanitary work areas.
  • Verify patient information and label drug and research Investigator product correctly.
  • Review CRC schedule, verify, and complete orders in the electronic medical record and/or clinical trial manager system.
  • Deliver investigator product and related materials to clinics and study participants, as required. Complete and assist with Investigator product inventory, master log drug accountability.
  • Follow all health and safety protocols and procedures to maintain sanitary work areas.
  • Verify patient information and label drug and research Investigator product correctly.
  • Review CRC schedule, verify, and complete orders in the electronic medical record and / or clinical trial manager system.
  • Preparation of investigational product and standard of care drugs for dispensation and infusion.
  • Specialized functions/areas include but are not limited to the following: sterile compounding, medication history, inventory control, medication maintenance, unit inspection and packaging.
  • Utilizes requisite equipment, non-sterile and/or compounding supplies and computer systems as appropriate for the procurement, preparation for verification and/or delivery of medication.
  • Performs quality control procedures and contributes to the maintenance of the pharmacy, equipment, and supplies.
  • Receives investigational drug supplies, handles return, and removes from stock investigational drugs from completed studies; dispenses study investigational drug, maintain drug inventory, and review expiration dates.
  • Records temperatures daily if assigned, contacts study coordinators for clarifications and excursions.
  • Ensure compliance to institutional, state, and federal regulatory policies.
  • Organize and manage documents and materials – sorting, labeling, filing, discarding per facility SOPs.
  • Answering research queries as designated by CRC’s. Assist with subject accountability and compliance.
  • Assist regulatory department in filing and maintaining pharmacy binder.
  • Participate in the training and orientation of new pharmacy technicians.
  • Perform all other duties as assigned. Work with providers and clinical research coordinators and following their directions.

Knowledge, Skills, and Abilities

  • Ability to work independently with minimal day-to-day supervision.
  • Detail-oriented and committed to ensuring patient confidentiality.
  • Excellent motor skills and the ability to stand for long periods of time.
  • Advanced written and verbal communication skills.
  • Data entry and computer skills.
  • Thorough understanding of clinical research requirements, principles of GCP, and biomedical research ethics. Must be GCP and IATA certified.
  • Excellent interpersonal and communication skills.
  • Ability to interact effectively with professional and administrative staff, sponsor, regulator representatives, patients, potential subjects, and referral sources.
Source · Arizona Liver HealthFirst seen 11 NovOriginal ↗