As the Research Pharmacy Technician you will assist the Research Pharmacist in all aspects of clinical trial drug management. You will be required to have knowledge of protocol-specific drug information including admixture guidelines, drug stability data as well as drug transport and shipping instructions. You will have a working knowledge of federal regulations related to the use of the investigational drugs as outlined in the Code of Federal Regulations including, but not limited to, documentation guidelines. You will be responsible for drug inventory and maintaining temperature logs. With Research Pharmacist supervision, you will sign out, prepare and dispense investigational and commercially provided drugs. 

• You will review protocols and determine clinical and drug supply needs  

• You will order corresponding supplies from approved vendor(s) and sponsor organization(s)  

• You will maintain drug logs and manage inventory to assure adequate and accurate inventory levels  

• You will use appropriate IVRS system for study drug assignment and receipt  

• You will maintain temperature logs (ambient, refrigerator and freezer) to assure proper drug storage  

• You will prepare, labels and packages oral or intravenous investigational study agent(s) with pharmacist supervision 

• You will package sponsor-provided commercial study agent(s) with pharmacist supervision 

• You will assist Pharmacist in documenting and maintaining master drug logs 

You should have for this position: 

• A High School Diploma, preferably a Bachelor’s Degree 

• Pharmacy Technician certification 

• The ability to work in a fast paced environment while maintaining attention to detail  

• The ability to organize daily activities effectively with ability to move from task to task during the day  

• The ability to communicate clearly to other team members as well as industry sponsors 

• At least one year of experience working as a Pharmacy Technician  

• IV Admixture experience is preferred 

• Chemotherapy Admixture experience is preferred 

About Sarah Cannon Research Institute

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials. Focused on advancing therapies for patients over the last three decades, SCRI is a leader in drug development. In 2022, SCRI formed a joint venture with former US Oncology Research to expand clinical trial access across the country. It has conducted more than 750 first-in-human clinical trials since its inception and contributed to pivotal research that has led to the majority of new cancer therapies approved by the FDA today. SCRI’s research network brings together more than 1,300 physicians who are actively enrolling patients into clinical trials at more than 250 locations in 24 states across the U.S. Please click here to learn more about our research offerings.

We care about the well-being of the patients and communities we serve, and that starts with caring for our people. That’s why we have a Total Rewards package that includes comprehensive benefits to support physical, mental, and financial well-being. Our Total Rewards offerings serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves. For more information regarding benefits through our parent company, McKesson, please click here.

As part of Total Rewards, we are proud to offer a competitive compensation package. This is determined by several factors, including performance, experience and skills, equity, regular job market evaluations, and geographical markets. In addition to base pay, other compensation, such as an annual bonus or long-term incentive opportunities may be offered.