Research Pharmacy Manager We are seeking a dedicated and experienced Research Pharmacy Manager to join our client’s innovative team. This full-time role offers the opportunity to lead and manage pharmaceutical research within oncology trials. You will work closely with healthcare professionals, clinical researchers, and patients to ensure the safe and effective application of pharmaceutical treatments in cutting-edge oncology studies. As the Research Pharmacy Manager, you will play a vital role in overseeing drug therapy management, ensuring compliance with regulatory guidelines, and supporting the integration of research findings into clinical practice. Your expertise will be key in driving successful outcomes in oncology research trials, contributing to the advancement of cancer treatment. If you're passionate about making a meaningful impact in the field of oncology and looking for a leadership role in research pharmacy, we encourage you to apply today! Responsibilities: • Medication Oversight: Evaluate oncology and chemotherapy treatments for clinical trial participants, ensuring accurate dosing, administration, and managing potential side effects. Supervise the preparation and distribution of chemotherapy medications within acute care environments. • Clinical Research Collaboration: Provide expert pharmacological advice and support for oncology-focused clinical trials, ensuring compliance with Good Clinical Practice (GCP) and all applicable regulatory standards. Prior experience in clinical research is a plus but not essential. • Adverse Event Monitoring: Track, document, and report any adverse events (AEs), severe adverse events (SAEs), adverse drug reactions (ADRs), medication errors, and drug interactions associated with investigational products in clinical trials. • Regulatory Adherence: Assist in the development, review, and compliance with study protocols, ensuring adherence to regulations, particularly in relation to investigational drug management and regulatory inspections. • Cross-Functional Collaboration: Partner with oncologists, research coordinators, nurses, and other healthcare professionals to ensure excellent patient care and clinical trial outcomes, while also attending related clinical meetings. • Patient Education: Provide patients with clear information regarding their medication schedules, potential risks, benefits, and strategies for managing any side effects within the context of clinical trials. • Data Management & Analysis: Contribute to the process of collecting, analyzing, and preparing data for clinical study reports, scientific publications, and regulatory submissions. • Ongoing Education: Continuously update your knowledge of oncology treatments, clinical trial methodologies, and pharmaceutical research advancements through professional development opportunities, training, and conferences. Qualifications: Education: Doctor of Pharmacy (PharmD) degree from an accredited school of pharmacy. Licensing: Valid and active pharmacist license in California. Experience: • At least 2 years of experience in oncology pharmacy practice. • Experience in working with investigational drugs, chemotherapy regimens, and oncology clinical research is preferred. Certifications & Residency (Preferred but not required): • Board Certification in Oncology Pharmacy (BCOP) is highly desirable (especially for consideration in the higher salary range). • ASHP-accredited PGY-1 and PGY-2 residency in oncology or pain management is a plus. • Clinical Research Certification (ACRP or SOCRA) is an added benefit. Knowledge & Skills: • Deep understanding of oncology pharmacotherapy, including chemotherapy, biologics, targeted therapies, and immunotherapy. • Excellent communication, organizational, and collaboration skills, with a strong focus on interpersonal effectiveness. • Familiarity with clinical trial protocols, regulatory guidelines, and ethical standards is preferred. • Proficiency in using EHR/EMR systems and clinical trial management software is an advantage. Personal Attributes: • Exceptional attention to detail with the ability to juggle multiple projects effectively. • Strong ability to work independently and within a collaborative research team. • Demonstrated commitment to patient safety and continuously improving healthcare outcomes. Working Conditions: • Full-time position, Monday through Friday, 9:00 AM to 5:00 PM with occasional travel (less than 10%) and potential overtime based on study needs. • Work is performed in a clinical research environment, with direct patient interaction, in a hospital or outpatient clinic. Compensation: $139,000 - $199,000 yearly

• Medication Oversight: Evaluate oncology and chemotherapy treatments for clinical trial participants, ensuring accurate dosing, administration, and managing potential side effects. Supervise the preparation and distribution of chemotherapy medications within acute care environments. • Clinical Research Collaboration: Provide expert pharmacological advice and support for oncology-focused clinical trials, ensuring compliance with Good Clinical Practice (GCP) and all applicable regulatory standards. Prior experience in clinical research is a plus but not essential. • Adverse Event Monitoring: Track, document, and report any adverse events (AEs), severe adverse events (SAEs), adverse drug reactions (ADRs), medication errors, and drug interactions associated with investigational products in clinical trials. • Regulatory Adherence: Assist in the development, review, and compliance with study protocols, ensuring adherence to regulations, particularly in relation to investigational drug management and regulatory inspections. • Cross-Functional Collaboration: Partner with oncologists, research coordinators, nurses, and other healthcare professionals to ensure excellent patient care and clinical trial outcomes, while also attending related clinical meetings. • Patient Education: Provide patients with clear information regarding their medication schedules, potential risks, benefits, and strategies for managing any side effects within the context of clinical trials. • Data Management & Analysis: Contribute to the process of collecting, analyzing, and preparing data for clinical study reports, scientific publications, and regulatory submissions. • Ongoing Education: Continuously update your knowledge of oncology treatments, clinical trial methodologies, and pharmaceutical research advancements through professional development opportunities, training, and conferences.