Laboratory Technician

About the Role

As a Lab Technician, you will perform high-level medical laboratory processing procedures for specimens received from patients enrolled in clinical trials. You will initiate improvements, tools, processes, and forms to enhance the efficiency and quality of work in the lab.

Responsibilities

• Expertly process and ship pharmacokinetic/pharmacodynamic and all other samples according to instructions provided by the study sponsor.
• Become the primary processor and trainer for high-level processing procedures requested by study sponsors.
• Attend the lab portion of the site initiation visit (SIV) when possible.
• Provide assistance in understanding a lab manual when required.
• Prepare study supplies and source documents necessary for obtaining lab samples prior to patient treatment.
• Utilize the electronic medical record (EMR) for source documentation.
• Maintain accurate freezer sample logs and records of sample acquisition and shipping. Ensure all PK samples have source documents available in patient charts that are accurate and complete. Maintain all shipping and processing records in the patient’s study folder.
• Schedule appropriate couriers for sample shipments and ensure an adequate supply of dry ice is available.
• Respond to queries generated from the study sponsor or contract lab regarding patient/sample data.
• Maintain laboratory equipment and workspace in all areas.
• Interface with research nurses to ensure all research patients have correct lab kits prior to visits and that all necessary specimens are collected per the lab manual.

Requirements

• Vocational or technical training in laboratory process and/or phlebotomy.
• A current BLS certification.
• Knowledge of organization policies, procedures, and systems.
• Knowledge of OSHA requirements for safe handling of blood and body fluids.
• Experience gathering and reporting information.
• Experience in venipuncture and blood processing.
• Ability to multi-task in a fast-paced environment.
• Ability to work effectively with staff and other internal and external sponsors and agencies.
• At least one year of clinical laboratory and phlebotomy or equivalent experience.

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 850 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 in the past decade.

SCRI’s research network brings together more than 1,300 physicians who are enrolling patients into clinical trials at more than 200 locations in 20+ states across the U.S.

Benefits

We care about the well-being of the patients and communities we serve, and that starts with caring for our people. Our Total Rewards package includes comprehensive benefits to support physical, mental, and financial well-being. Offerings are designed to serve the different needs of our diverse colleague population and ensure they are the healthiest versions of themselves.

Pay

We offer a competitive compensation package determined by several factors, including performance, experience, 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.