Research Pharmacist

Parexel•Glendale, CA

2d•Onsite

About The Position

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Research Pharmacist – Early Phase Clinical Unit Location: Glendale, California Bring Your Purpose to Parexel At Parexel, we simplify the journey from science to new treatments with a deep commitment to patients and quality. Our Early Phase Clinical Unit in Glendale is seeking a Research Pharmacist who brings scientific rigor, operational excellence, and a passion for advancing clinical research. I What You’ll Do Lead & Collaborate Supervise pharmacy coordinators and technicians, ensuring accuracy and adherence to standards. Serve as a Sub‑Investigator, supporting clinical and scientific monitoring. Act as a key liaison between Parexel, AHGL Pharmacy, and hospital leadership. Drive Excellence in Investigational Product Management Oversee all medication handling in alignment with GCP, SOPs, and regulatory requirements. Communicate with Sponsors on drug shipment, accountability, and dispensation. Manage inventory, blinding/randomization, and documentation. Dispense study medications and review concomitant medications for safety and eligibility. Support medication management for study participants at Adventist Health Glendale. Champion Quality & Compliance Ensure the research pharmacy meets all hospital licensing and regulatory standards. Oversee QC/QA processes, drug storage, temperature logs, and accountability forms. Review IRB submissions, amendments, progress reports, and adverse event documentation. Represent Parexel at IRB and regulatory compliance meetings. Provide protocol interpretation and feasibility insights for new studies. Support Training & Continuous Improvement Lead training on departmental and cross‑functional SOPs. Identify opportunities for process improvement and drive measurable outcomes. Maintain and reinforce GCP knowledge across the team. Contribute to scientific outputs such as abstracts, manuscripts, and presentations.

Requirements

Pharm.D or RPh with an active California pharmacist license.
2–5 years of experience in clinical research or hospital pharmacy preferred.
Expertise in sterile and non‑sterile compounding and investigational drug management.
Strong communication skills, meticulous attention to detail, and a patient‑first mindset.
Ability to manage multiple priorities with accuracy and enthusiasm.
Proficiency in MS Word, Excel, Outlook; familiarity with clinical trial systems.
Solid understanding of GCP and relevant regulatory frameworks.

Responsibilities

Supervise pharmacy coordinators and technicians, ensuring accuracy and adherence to standards.
Serve as a Sub‑Investigator, supporting clinical and scientific monitoring.
Act as a key liaison between Parexel, AHGL Pharmacy, and hospital leadership.
Oversee all medication handling in alignment with GCP, SOPs, and regulatory requirements.
Communicate with Sponsors on drug shipment, accountability, and dispensation.
Manage inventory, blinding/randomization, and documentation.
Dispense study medications and review concomitant medications for safety and eligibility.
Support medication management for study participants at Adventist Health Glendale.
Ensure the research pharmacy meets all hospital licensing and regulatory standards.
Oversee QC/QA processes, drug storage, temperature logs, and accountability forms.
Review IRB submissions, amendments, progress reports, and adverse event documentation.
Represent Parexel at IRB and regulatory compliance meetings.
Provide protocol interpretation and feasibility insights for new studies.
Lead training on departmental and cross‑functional SOPs.
Identify opportunities for process improvement and drive measurable outcomes.
Maintain and reinforce GCP knowledge across the team.
Contribute to scientific outputs such as abstracts, manuscripts, and presentations.