Clinical Pharmacist, Investigational Drug Section

The START Center for Cancer Research

$185K — $195K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Graduate of an ACPE accredited School of Pharmacy
  • Current State pharmacy license
  • Previous experience in hospital or clinic pharmacy settings
  • Knowledge of sterile compounding requirements for chemotherapy agents
  • Proficient in Microsoft Office and electronic medical record systems
  • Familiar with Good Clinical Practice (GCP) principles

Responsibilities

  • Verify medication orders for investigational drugs and chemotherapy agents
  • Supervise preparation and dispensing of medications, ensuring compliance with verification processes
  • Provide patient counseling and drug information to healthcare team and patients
  • Oversee drug inventories and associated documentation
  • Assist staff in maintaining investigational documentation and inventory records
  • Review and understand clinical trial protocols and amendments
  • Maintain accountability reports for investigational drugs

Benefits

  • Collaborative and autonomous work environment
  • Professional development opportunities
  • Supportive team dynamics
  • Engagement in cutting-edge clinical trials
  • Contribution to patient care in an impactful field
Full Job Description
We are seeking a Clinical Pharmacist, Investigational Drug Section. The Clinical Pharmacist, Investigational Drug Section (IDS) is responsible for all facets of medication order verification, dispensing and documentation process for investigational drugs, conventional chemotherapy and supportive care medications provided by the IDS. The pharmacist may be involved in the provision of pharmaceutical care including assisting with patient interviews, maintenance of current medication lists, providing patient medication education, providing drug information to the healthcare team and patients. The pharmacist will practice with a high degree of autonomy, guided by IDS SOPs and quality assurance verification guidelines. This role is responsible for the daily supervision of staff assigned to medication preparation, dispensing, and operation of the IDS in accordance with all applicable rules and regulations.

The salary range for this role is $ 185,000- $195,000.00 However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience.

Work Schedule: Monday through Friday 7 a.m. - 5 p.m. or 8 a.m. - 6 p.m.

Location: START Los Angeles: 10700 Santa Monica Blvd, Suite 310, Los Angeles, CA 90025

Essential Responsibilities:
  • Verify medication orders including accuracy of dosages and calculations, review of basic patient eligibility criteria, including but not limited to accurately signed / dated study consent form(s), laboratory values within treatment criteria, all appropriate tests have been completed, resolution of known toxicity from previous chemotherapy, and an absence of serious known drug interactions.
  • Oversee the preparation and dispensing of all medications from the IDS, including supervision of certified pharmacy technicians during preparation of IV admixtures and oral medication dosages, insuring compliance with all steps of the double-check verification process prior to releasing dosages from the IDS.
  • Provide pharmaceutical care including patient medication and supportive care counseling, and drug information to the healthcare team and patients.
  • Oversee drug inventories including documentation of current inventory, projection of expected usage in concert with ordering, receiving, storage and dispensation tracking of Phase I and conventional medications.
  • Assist pharmacy technicians in maintaining adequate investigational documentation, records, weekly inventory, and interactions with study personnel
  • Review new protocol(s), protocol amendments and associated forms.
  • Maintain and generate reports using the IDS drug accountability program.
  • Contribute to the effective operation of the pharmacy department. Enter accurate medication computer order entries and accurate maintenance of reported patient home medications in the EMR.
  • Other duties may be assigned at any time.


Education & Experience:
  • Graduate of an ACPE accredited School of Pharmacy.
  • Current State license.
  • Previous hospital/clinic pharmacy experience.
  • Familiarity with sterile compounding requirements for chemotherapy agents, USP, USP, laminar airflow hood(s) / biological safety cabinet(s); telephone and copier / scanner / facsimile machine.
  • Computer skills, including use Microsoft Office products, including Word, Excel, Power Point and Access.
  • Familiarity with the use of electronic medical record program(s), pharmacy software programs and study IRT systems.
  • Knowledge of Good Clinical Practice (GCP) principles.


Preferred Education and Experience:
  • Sterile compounding & chemotherapy certification.
  • Intravenous sterile product training.
  • Prior experience in clinical trials and management of investigational drugs.
  • Specialty residency in oncology and/or current BPS Board Certified Oncology Pharmacist (BCOP).
  • Bilingual.


Physical and Travel Requirements:
  • 80% of time spent standing and/or walking.
  • Ability to lift up to a 25-pound weight load.
  • Some lifting and bending, pushing and/or pulling loads.

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