Investigational Drug Services (IDS) Pharmacist, On-site

IQVIA LLC; Irving (TX); On-site; USD 57,700 - 209,800; Full time

Benefits offered by this job

Health and welfare benefits

Incentive plans and bonuses

Job summary

IQVIA LLC is seeking an IDS Pharmacist to join our Irving, TX Clinical Research Site focusing on Phase 1 Oncology trials. This full-time, on-site role encompasses ensuring protocol integrity and patient safety throughout clinical trials. Responsibilities include reviewing and complying with protocols, overseeing medication dispensing, managing investigational product inventories, supervising technicians, and facilitating staff training. A Current Pharmacy License in Texas is essential, with preferred IV and Chemotherapy certifications. Opportunities for impactful work in advancing cancer research await you.

Qualifications

• Current Pharmacy License in Texas or Virginia is required.
• Pharmacy Preceptor License and IV Certification are preferred.
• Strong knowledge of GCP, GMP, USP <797> and <800>.

Responsibilities

• Ensure protocol compliance and attend site initiation visits.
• Oversee compounding of investigational products.
• Supervise IDS technicians and maintain SOP compliance.

Skills

Knowledge of GCP

Knowledge of GMP

IV Certification

Chemotherapy Certification

Manual dexterity

Education

Current Pharmacy License in Texas

Pharmacy Preceptor License

Job description

Investigational Drug Services (IDS) Pharmacist, On-site page is loaded## Investigational Drug Services (IDS) Pharmacist, On-sitelocations: Irving, TX: Garland, TX: Dallas, TXtime type: Full timeposted on: Posted Todayjob requisition id: R1522224The team within NEXT Oncology (an Avacare Business) is seeking a dedicated **IDS Pharmacist** to join our **Irving, TX** Clinical Research Site **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 <797> and <800>.* **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 <797> and <800>**, and clinical trial regulations* Ability to lift up to 40 lbs and perform duties requiring manual dexterity and extended periods of sitting/standingAt 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. Learn more atIQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.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.IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.