Pharmacy Graduate Intern
San Antonio, TX - USA
Job Summary
Job Summary
This position provides hands-on experience in the preparation documentation and managementof investigational products for clinical trials. The intern will work under the direct supervision ofa licensed pharmacist to support study start-up dispensing inventory and documentationprocesses 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:
Assist in the development preparation and maintenance of protocol-specific documents
including:
Compounding worksheets
Drug accountability logs
Patient medication diaries
Dosing instructions
Visit-specific medication handouts or counseling sheets
Format and print protocol materials for staff and participants; maintain documentversion control.
Support setup of study binders electronic files and documentation templates for eachtrial.
Dispensing & Inventory:
Assist in the preparation labeling and dispensing of investigational drugs per protocol
and Good Clinical Practice (GCP) guidelines.
Help manage inventory tracking including receiving study drug shipments logging lot
numbers expiration dates and storage conditions.
Monitor refrigerator/freezer logs and report temperature excursions promptly.
Reconcile drug inventory and assist with preparing drug return or destruction forms.
Participant & Study Support:
Provide study participants with protocol-specific medication instructions and review
diary completion processes under pharmacist supervision.
Communicate with clinical coordinators and nurses regarding drug availability and
dosing schedules.
Assist in packaging take-home medication kits for participants in compliance with study
requirements.
Regulatory Compliance:
Maintain accurate real-time documentation for investigational drug accountability.
Support compliance with FDA IRB sponsor and Virginia Board of Pharmacy regulations.
Participate in internal audits and assist with documentation for sponsor monitoringvisits.
Knowledge Skills and Abilities
Strong written and verbal communication skills.
Excellent attention to detail and documentation accuracy.
Interest in community-based clinical research public health or investigational drugservices.
Proficient with Microsoft Word Excel and PDF editing tools for document preparation.
Ability to work independently and collaboratively in a small mission-driven teamenvironment.
Required Education and Experience
Education:
Currently enrolled in an ACPE-accredited PharmD program.
Must be in good academic standing and eligible for internship experience in a clinicalresearch setting.
Current IV Certification (required)
Licensure:
Current Pharmacy Intern License (required) in the state where the NEXT
Oncology position is located.
Preferred Qualifications:
Previous experience in a pharmacy research or clinical setting.
Familiarity with clinical trial operations GCP or IND processes.
Coursework or interests related to pharmacotherapy research ethics or public health.
Learning and Development Opportunities
Experience supporting real-world community-focused clinical trials.
Hands-on exposure to investigational drug handling documentation and regulatory compliance.
Opportunity to contribute to health equity and translational research efforts in
underserved populations.
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. 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 $33000.00 - $82600.00. 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.Required Experience:
Intern
About Company
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more