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Parexel

End-to-end clinical trials and regulatory consulting

Research Pharmacist

PharmacyConfirmed live in the last 24 hours
Part-timeGlendale, CA, USA$83 /hrIn-person

About the Job

Requirements

  • Pharm.D. or RPh and an active California pharmacist license.
  • Two to five years of experience in clinical research or hospital pharmacy is preferred.
  • Expertise in sterile and non-sterile compounding and investigational drug management.
  • Proficiency in Microsoft Word, Excel, and Outlook, and familiarity with clinical trial systems.
  • A solid understanding of Good Clinical Practice and relevant regulatory frameworks.
  • Ability to manage multiple priorities accurately.

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 medication handling in alignment with Good Clinical Practice, standard operating procedures, and regulatory requirements.
  • Communicate with Sponsors regarding drug shipment, accountability, and dispensation.
  • Manage inventory, blinding and 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 hospital licensing and regulatory standards.
  • Oversee quality control and quality assurance processes, drug storage, temperature logs, and accountability forms.
  • Review Institutional Review Board submissions, amendments, progress reports, and adverse event documentation.
  • Represent Parexel at Institutional Review Board and regulatory compliance meetings.
  • Provide protocol interpretation and feasibility insights for new studies.
  • Lead training on departmental and cross-functional standard operating procedures.
  • Identify process-improvement opportunities and drive measurable outcomes.
  • Maintain and reinforce Good Clinical Practice knowledge across the team.
  • Contribute to scientific outputs such as abstracts, manuscripts, and presentations.

Desired Qualifications

  • Two to five years of experience in clinical research or hospital pharmacy is preferred.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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