Investigational Pharmacist Opportunity Join a research-focused organization committed to advancing the future of medicine. As an Investigational Pharmacist, you will support the execution of clinical trials by ensuring accuracy, regulatory compliance, and exceptional standards of patient safety. Your clinical expertise and attention to detail will directly contribute to the development of innovative therapies that improve patient outcomes. In this full-time position, you will work closely with investigators, clinicians, and study coordinators to manage investigational products throughout the entire research process. This includes preparation, labeling, documentation, and accountability for all study medications. You will help maintain protocol integrity, oversee inventory and chain of custody, and ensure proper storage and dispensing practices that promote safety and regulatory adherence. Ideal candidates bring strong clinical knowledge, a commitment to ethical research practices, and the ability to collaborate effectively in a multidisciplinary environment. Experience in clinical research or investigational pharmacy is beneficial, though not required, for individuals with the right foundation and mindset. If you are motivated by precision, patient safety, and contributing to meaningful scientific progress, this is an opportunity to make a significant impact within a respected research team. Responsibilities: • Medication Oversight: Ensure proper dosing and administration of oncology treatments, manage side effects, and supervise chemotherapy medication preparation in acute care settings. • Clinical Research Collaboration: Provide pharmacological support for oncology trials, ensuring compliance with regulatory standards. • Adverse Event Monitoring: Track and report adverse events, drug reactions, and interactions related to investigational products. • Regulatory Adherence: Assist with protocol development and ensure compliance with investigational drug management regulations. • Cross-Functional Collaboration: Work closely with oncologists, nurses, and research staff to ensure patient care and successful trial outcomes. • Patient Education: Educate patients on medication regimens, risks, benefits, and side effect management. • Data Management & Analysis: Support data collection, analysis, and report preparation for clinical studies and regulatory submissions. • Ongoing Education: Stay updated on oncology treatments and clinical trial advancements through professional development. Qualifications: • Education: Doctor of Pharmacy (PharmD) from an accredited pharmacy school. • Licensing: Active pharmacist license in California. • Experience: Minimum of 2 years 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) is highly desirable. • ASHP-accredited PGY-1 and PGY-2 residency in oncology or pain management is a plus. • Clinical Research Certification (ACRP or SOCRA) is beneficial. • **Knowledge & Skills: **Strong understanding of oncology pharmacotherapy, including chemotherapy, biologics, targeted therapies, and immunotherapy. • Excellent communication, organizational, and collaboration skills. • Familiarity with clinical trial protocols, regulatory guidelines, and ethical standards is preferred. • Proficiency in EHR/EMR and clinical trial management software is advantageous. • Personal Attributes: Exceptional attention to detail and the ability to handle multiple projects. • Strong independent work ethic while collaborating effectively with research teams. • Commitment to patient safety and continuous healthcare improvement. • Working Conditions: Full-time, Monday to Friday, 9:00 AM to 5:00 PM, occasional travel (less than 10%), and potential overtime based on study needs. • Work in clinical research settings with direct patient interaction, either in hospitals or outpatient clinics. • Must reside in Southern California. Salary listed reflects the maximum amount, dependent on experience (DOE) Compensation: $195,000 yearly

• Medication Oversight: Ensure proper dosing and administration of oncology treatments, manage side effects, and supervise chemotherapy medication preparation in acute care settings. • Clinical Research Collaboration: Provide pharmacological support for oncology trials, ensuring compliance with regulatory standards. • Adverse Event Monitoring: Track and report adverse events, drug reactions, and interactions related to investigational products. • Regulatory Adherence: Assist with protocol development and ensure compliance with investigational drug management regulations. • Cross-Functional Collaboration: Work closely with oncologists, nurses, and research staff to ensure patient care and successful trial outcomes. • Patient Education: Educate patients on medication regimens, risks, benefits, and side effect management. • Data Management & Analysis: Support data collection, analysis, and report preparation for clinical studies and regulatory submissions. • Ongoing Education: Stay updated on oncology treatments and clinical trial advancements through professional development.