Investigational Drug Services (IDS) Pharmacist, On-site

IDS Pharmacist

The team within NEXT Oncology (an Avacare Business) is seeking a dedicated IDS Pharmacist to join our Irving, TX and Fairfax, VA Clinical Research Sites focused on Phase 1 Oncology trials. This is a fully on-site position supporting investigational drug services in a fast-paced, patient-centered research environment. The IDS Pharmacist plays a critical role in ensuring protocol integrity, patient safety, and regulatory compliance throughout the conduct of clinical trials.

Key Responsibilities

• Protocol Compliance: Review protocols, amendments, and study-specific documentation; attend site initiation visits; ensure accurate medication screening and documentation.

• Medication Dispensing & Preparation: Verify dosing accuracy, oversee compounding of investigational products (IP), and ensure compliance with USP and clinical trial regulations.

• IP Management & Accountability: Maintain inventory, manage drug receipt and returns, ensure proper documentation in Vestigo, and support monitoring visits.

• Administrative & Supervisory Duties: Supervise IDS technicians, maintain SOP compliance, support audits, and contribute to staff training and performance evaluations.

• Education & Training: Orient new staff and maintain required certifications and licenses.

• Data & Document Management: Upload and manage protocol documentation and staff credentials in eDOCs and Vestigo.

Minimum Requirements

• Current Pharmacy License in Texas or Virginia (required)

• Pharmacy Preceptor License (preferred)

• IV Certification (preferred)

• Chemotherapy Certification (preferred)

• Strong knowledge of GCP, GMP, USP and clinical trial regulations

• Ability to lift up to 40 lbs and perform duties requiring manual dexterity and extended periods of sitting/standing

Why Join Us?

At NEXT Oncology, you'll be part of a mission-driven team advancing cancer research and patient care. This role offers the opportunity to work closely with leading investigators and contribute meaningfully to clinical trials in a supportive and collaborative environment.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $57,700.00 - $209,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.