Pharmacy Graduate Intern

Job Summary This position provides hands-on experience in the preparation, documentation, and management of investigational products for clinical trials. The intern will work under the direct supervision of a licensed pharmacist to support study start-up, dispensing, inventory, and documentation processes, while gaining exposure to community-engaged clinical research. Essential Duties and Responsibilities Essential and other important responsibilities and duties may include but are not limited to the following: Study Start-Up & Documentation: u2022 Assist in the development, preparation, and maintenance of protocol-specific documents, including: u2022 Compounding worksheets u2022 Drug accountability logs u2022 Patient medication diaries u2022 Dosing instructions u2022 Visit-specific medication handouts or counseling sheets u2022 Format and print protocol materials for staff and participants; maintain document version control. u2022 Support setup of study binders, electronic files, and documentation templates for each trial. Dispensing & Inventory: u2022 Assist in the preparation, labeling, and dispensing of investigational drugs per protocol and Good Clinical Practice (GCP) guidelines. u2022 Help manage inventory tracking, including receiving study drug shipments, logging lot numbers, expiration dates, and storage conditions. u2022 Monitor refrigerator/freezer logs and report temperature excursions promptly. u2022 Reconcile drug inventory and assist with preparing drug return or destruction forms. Participant & Study Support: u2022 Provide study participants with protocol-specific medication instructions and review diary completion processes under pharmacist supervision. u2022 Communicate with clinical coordinators and nurses regarding drug availability and dosing schedules. u2022 Assist in packaging take-home medication kits for participants in compliance with study requirements. Regulatory Compliance: u2022 Maintain accurate, real-time documentation for investigational drug accountability. u2022 Support compliance with FDA, IRB, sponsor, and Virginia Board of Pharmacy regulations. u2022 Participate in internal audits and assist with documentation for sponsor monitoring visits. Knowledge Skills and Abilities u2022 Strong written and verbal communication skills. u2022 Excellent attention to detail and documentation accuracy. u2022 Interest in community-based clinical research, public health, or investigational drug services. u2022 Proficient with Microsoft Word, Excel, and PDF editing tools for document preparation. u2022 Ability to work independently and collaboratively in a small, mission-driven team environment. Required Education and Experience Education: u2022 Currently enrolled in an ACPE-accredited PharmD program. u2022 Must be in good academic standing and eligible for internship experience in a clinical research setting. Licensure: u2022 Must possess an active Pharmacy Intern Registration issued by the Texas Board of Pharmacy. Preferred Qualifications: u2022 Previous experience in a pharmacy, research, or clinical setting. u2022 Familiarity with clinical trial operations, GCP, or IND processes. u2022 Coursework or interests related to pharmacotherapy, research ethics, or public health. Learning and Development Opportunities u2022 Experience supporting real-world, community-focused clinical trials. u2022 Hands-on exposure to investigational drug handling, documentation, and regulatory compliance. u2022 Opportunity to contribute to health equity and translational research efforts in underserved populations. u2022 Mentorship and training by clinical research pharmacists and study staff 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 at IQVIA 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 $33,000.00 - $82,600.00. 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. EEO Minorities/Females/Protected Veterans/Disabled

Created: 2026-04-01