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

1-3 years
$57,700 – $144,100,
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) Pharmacist – Full-Time | On-Site | Fairfax, Virginia

Location: Fairfax, Virginia
Job Type: Full-Time, Office-Based
Job ID: R1511945

NEXT Oncology is seeking an experienced and detail-oriented Investigational Drug Services (IDS) Pharmacist to join its expanding clinical research team in Fairfax, Virginia. This fully on-site role supports Phase 1 oncology research programs and plays a key part in ensuring investigational product integrity, patient safety, and regulatory compliance.

Position Overview

The IDS Pharmacist will work within a high-performing research environment, overseeing investigational product management, ensuring compliance with clinical trial protocols, and supporting operational workflows critical to early-phase oncology studies.

Key Responsibilities

Protocol Compliance

  • Review clinical trial protocols, amendments, and study-related documentation.

  • Participate in Site Initiation Visits and ensure proper medication screening and documentation.

  • Maintain strict adherence to GCP, GMP, and protocol requirements.

Medication Dispensing & Preparation

  • Verify dosing accuracy for investigational products.

  • Oversee sterile compounding and preparation processes in compliance with USP <797> and USP <800> standards.

  • Maintain accurate dispensing and preparation records.

Investigational Product (IP) Management

  • Manage inventory control, including drug receipt, storage, accountability, and returns.

  • Document all activities in Vestigo and support monitoring and audit visits.

  • Ensure full compliance with regulatory and sponsor requirements.

Administrative & Supervisory Responsibilities

  • Supervise IDS pharmacy technicians and ensure adherence to SOPs.

  • Assist with internal audits, quality checks, and performance evaluations.

  • Support training and onboarding of new staff members.

Data & Document Management

  • Maintain protocol documentation, staff licenses, and certifications within eDOCs and Vestigo.

  • Support accurate reporting, recordkeeping, and compliance management.

Minimum Experience & Requirements

  • Active Pharmacy License in Virginia (required)

  • Pharmacy Preceptor License (preferred)

  • IV Certification (preferred)

  • Chemotherapy Certification (preferred)

  • Minimum 1–3 years of experience in hospital pharmacy, investigational drug services, or clinical research pharmacy

  • Proficiency in GCP, GMP, USP <797>, USP <800>, and clinical trial regulatory requirements

  • Ability to lift up to 40 lbs, perform manual tasks, and stand or sit for extended periods

Why Join NEXT Oncology?

  • Work within a mission-driven organization advancing early-phase oncology research.

  • Collaborate with leading investigators and contribute to life-changing clinical trials.

  • Engage in a supportive, innovative, and patient-centered research environment.

About IQVIA

IQVIA is a global leader in clinical research, healthcare analytics, and life sciences technology solutions. The organization supports the development and commercialization of innovative medical treatments worldwide.

Compensation Range: Annualized base pay between $57,700 – $144,100, depending on experience, education, skills, and location. Additional incentives, bonuses, health benefits, and welfare programs may be offered based on the position.

IQVIA is an equal opportunity employer and considers all qualified applicants without regard to protected characteristics.