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Investigational Drug Services (Ids) Pharmacy Technician, On-Site, Fairfax, Virginia

1 years
$33,000 – $82,600
10 Nov. 21, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Investigational Drug Services (IDS) Pharmacy Technician

Full-Time | On-Site | Fairfax, Virginia | Job ID: R1511959**

Position Overview

A leading oncology research organization is seeking an experienced IDS Pharmacy Technician to support its Phase I clinical trials at the Fairfax, Virginia site. This full-time, office-based role offers a consistent Monday–Friday daytime schedule, providing an excellent balance between professional responsibilities and personal life while contributing to innovative oncology research.

This position is ideal for licensed pharmacy technicians with hands-on compounding experience who are looking to expand their expertise in investigational drug services within an advanced clinical research environment.

Key Responsibilities

Protocol & Clinical Compliance

  • Enter concomitant medications into the EMR system and prepare investigational products according to study protocols.

  • Ensure strict adherence to GCP, GMP, and all clinical research and pharmacy regulatory requirements.

Medication Preparation & Compounding

  • Compound intravenous and oral investigational products, including hazardous drugs, in compliance with USP <797> and USP <800> standards.

  • Maintain accuracy, sterility, and safety across all compounding processes.

Inventory & Accountability

  • Manage investigational product (IP) and conventional medication inventory using Vestigo and eDOCs.

  • Oversee documentation, ordering, storage, and drug accountability in accordance with protocol and regulatory requirements.

Administrative & Operational Support

  • Assist with audits, monitoring visits, SOP development, and site operational needs.

  • Provide team coverage when needed and support efficient daily operations.

Training & Documentation

  • Assist in onboarding new team members and ensure proper orientation to IDS workflows.

  • Maintain active certifications and support continuing education requirements.

  • Upload, manage, and track protocol documents, credentials, and compliance data in eDOCs and Vestigo.

Required Qualifications & Experience

  • Active Pharmacy Technician License in Virginia (required).

  • IV Certification with a minimum of 1 year of mixing/compounding experience (required).

  • Chemotherapy Certification with at least 6 months of chemo-mixing experience (required).

  • Strong knowledge of USP <797>, USP <800>, GCP, GMP, and oncology research processes.

  • Ability to lift up to 40 lbs and remain standing or walking for extended periods.

  • Prior experience in investigational drug services or clinical research pharmacy is preferred.

Why Join This Team

This role offers the opportunity to work in a mission-driven oncology research environment that prioritizes patient safety, scientific accuracy, and professional development. The IDS team is known for its supportive culture, collaborative approach, and commitment to excellence in clinical research operations.

Compensation

  • Annualized pay range: $33,000 – $82,600

  • Actual compensation may vary based on experience, education, skills, location, and schedule.

  • Additional benefits may include incentives, bonuses, and a comprehensive health and welfare package.

About the Employer

IQVIA is a global leader in clinical research, healthcare intelligence, and advanced analytics supporting the development and commercialization of innovative medical treatments. The organization promotes an inclusive and equitable work environment and welcomes applicants from all backgrounds and protected categories.