We are looking for a highly skilled and motivated Oncology Pharmacist to join our client's dynamic team on a full-time basis. In this role, you will collaborate closely with healthcare providers, clinical researchers, and patients to support innovative oncology clinical trials. Your expertise will be critical in ensuring the safe, effective, and evidence-based use of pharmaceutical therapies within oncology research. Responsibilities: • Medication Management : Assess chemotherapy and oncology medications for clinical trial patients, ensuring proper dosing, administration, and side effect management. Oversee compounding and dispensing of chemotherapy meds in acute care settings. • Clinical Research Support : Provide pharmacological guidance for oncology clinical trials, ensuring compliance with GCP and regulatory guidelines. Clinical research experience is preferred but not required. • Pharmacovigilance : Monitor and report adverse events (AEs), serious adverse events (SAEs), adverse drug reactions (ADRs), medication errors, and drug interactions for investigational products in clinical trials. • Regulatory Compliance : Assist in protocol preparation, review, and adherence, including investigational drug management and regulatory inspections. • Collaboration : Work with oncology investigators, research coordinators, nurses, and other professionals to ensure optimal patient care and study outcomes, attending relevant clinical meetings. • Patient Education : Educate patients on medication regimens, risks, benefits, side effects, and management strategies within the context of clinical trials. • Data Analysis & Reporting : Contribute to data collection, analysis, and preparation of clinical study reports, publications, and regulatory submissions. Qualifications: • Education : PharmD (Doctor of Pharmacy) from an accredited school of pharmacy. • Licensure : Active pharmacist license in California. • Experience : • Minimum of 2 years of experience in oncology pharmacy practice. • Experience with investigational drugs, chemotherapy regimens, and oncology clinical research preferred. • Certifications & Residency (preferred but not required): • Board Certification in Oncology Pharmacy (BCOP) highly desirable. • ASHP-Accredited PGY-1 and PGY-2 residency in oncology or pain management a plus. • Clinical Research Certification (ACRP or SOCRA) a plus. • Knowledge & Skills : • Strong knowledge of oncology pharmacotherapy, including chemotherapy, biologics, targeted therapies, and immunotherapy. • Strong communication, collaboration, organizational, and interpersonal skills. • Familiarity with clinical trial protocols, regulatory requirements, and ethical guidelines preferred. • Proficiency with EHR/EMR systems and clinical trial management software a plus. • Personal Attributes : • Strong attention to detail with the ability to manage multiple projects simultaneously. • Ability to work independently and collaboratively within a research team. • Demonstrated commitment to patient safety and improving healthcare outcomes. • Working Conditions : • Full-time, Monday to Friday, 9am-5pm with occasional travel ( • Medication Management: Assess chemotherapy and oncology medications for clinical trial patients, ensuring proper dosing, administration, and side effect management. Oversee compounding and dispensing of chemotherapy meds in acute care settings. • Clinical Research Support: Provide pharmacological guidance for oncology clinical trials, ensuring compliance with GCP and regulatory guidelines. Clinical research experience is preferred but not required. • Pharmacovigilance: Monitor and report adverse events (AEs), serious adverse events (SAEs), adverse drug reactions (ADRs), medication errors, and drug interactions for investigational products in clinical trials. • Regulatory Compliance: Assist in protocol preparation, review, and adherence, including investigational drug management and regulatory inspections. • Collaboration: Work with oncology investigators, research coordinators, nurses, and other professionals to ensure optimal patient care and study outcomes, attending relevant clinical meetings. • Patient Education: Educate patients on medication regimens, risks, benefits, side effects, and management strategies within the context of clinical trials. • Data Analysis & Reporting: Contribute to data collection, analysis, and preparation of clinical study reports, publications, and regulatory submissions. • Professional Development: Stay up-to-date on oncology treatments, clinical trial methods, and pharmacological research through continuing education and relevant training. Compensation: $140,000-$160,000 per year C-Clinical at Century City
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