Clinical Pharmacist, Investigational Drug Section

The START Center for Cancer Research (“START”) is the world’s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering\"Hope Through Access”tocutting edgetrials throughout the UnitedStatesand Europe. We areseekingaClinical Pharmacist, Investigational Drug Section.TheClinical Pharmacist, Investigational Drug Section(IDS)is responsible forallfacetsof medication order verification, dispensing and documentation process for investigational drugs, conventional chemotherapy and supportive care medications provided by the IDS. The pharmacistmay beinvolved 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 roleis responsible forthedaily supervision of staff assigned to medication preparation, dispensing, and operation of the IDSin accordance withall applicable rules and regulations. The salary range for this role is $165,000.00 -$175,000.00 However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience. Work Schedule: Monday through Friday: 7:30a.m to 4:30pm or 8am to 5pm. Location: 629 Cranbury Rd. East Brunswick, NJ 08816 Essential Responsibilities: Verifymedication 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. Overseethe preparation and dispensing of all medications from the IDS, including supervision of certified pharmacy technicians during preparation of IV admixtures and oral medication dosages,insuringcompliance with all steps of the double-check verification process prior to releasing dosages from the IDS. Provide pharmaceutical care including patient medication and supportive carecounseling, anddrug 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. Assistpharmacy technicians inmaintainingadequate investigational documentation, records, weekly inventory, and interactions with study personnel Review new protocol(s), protocolamendmentsand associated forms. Maintain and generate reports using the IDS drug accountability program. Contribute to the effective operation of the pharmacy department.Enteraccuratemedication computer order entries andaccuratemaintenance 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. Previoushospital/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, includinguseMicrosoftOffice products, including Word, Excel, Power Point and Access. Familiarity with the use of electronic medical record program(s), pharmacy softwareprogramsand study IRTsystems. Knowledge of Good Clinical Practice (GCP) principles. PreferredEducationandExperience: 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. PhysicalandTravelRequirements: 80% oftimespent standing and/or walking. Ability tolift upto a25-pound weight load. Some lifting and bending,pushingand/or pulling loads. Best-in-Class Benefits and Perks We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally: 401(k) retirement savings plan with employer match Eligibility for an annual performance bonus, based on role and company results Generous paid time off and paid holidays Comprehensive medical, dental, and vision coverageand optional insuranceoptions Company p‑aid life and disability insurance for added financial protection Employee Assistance Program (EAP) providing confidential, no ‑cost support for you and your family from day one Flexible FSA and HSA plans to support your financial wellness Commitment to a supportive environment that values balance, wellbeing, and flexibility We’recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you’lljoin a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. More About START START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. STARTrepresentsthe world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Learn more at STARTresearch.com. Ready to be part of a team changing the future of cancer treatment? Join us in our mission to conquer cancer, one clinical trial at a time. Yourexpertiseand dedication can help us bring hope and healing to patients worldwide. We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. #J-18808-Ljbffr START Center for Cancer Research