Laboratory Technician
Sarah Cannon Research Institute
Summary
As a Lab Technician you will perform high-level medical laboratory processing procedures for specimens received on patients enrolled in clinical trials.
Job description
- You will initiate improvements, tools, processes and forms to enhance the efficiency and the quality of work in the lab
- You will expertly process and ship pharmacokinetic/pharmacodynamic and all other samples according to instructions provided by study sponsor
- You will be responsible for high-level processing procedures requested by study sponsors becoming the primary processor and trainer for those procedures
- You will be responsible for attending the lab portion of the site initiation visit (SIV) when possible
- You will provide assistance in understanding a lab manual when required
- You will prepare study supplies/source documents necessary for obtaining lab samples prior to patient treatment
- You will utilize electronic medical record (EMR) for source documentation
- You will maintain accurate freezer sample logs
- You will maintain accurate records of sample acquisition and shipping. All PK samples must have source documents available in patient charts that are accurate and complete. All shipping and processing records should be maintained in the patient’s study folder
- You will schedule appropriate courier for sample shipments
- You will ensure there is an adequate supply of dry ice available for shipments
- You will have the ability to respond to queries generated from study sponsor or contract lab regarding patient/sample data
- You will maintain laboratory equipment and workspace in all areas
- You will interface with Research nurses to ensure that all research patients have correct lab kits prior to patients’ visits and to ensure all necessary specimens are collected per lab manual
Requirements
- Vocational or technical training in laboratory process and/or phlebotomy
- A current BLS certification
- Knowledge of organization policies, procedures systems
- Knowledge of OSHA requirements for safe handling of blood and body fluids
- Experience gathering and reporting information
- Experience in venipuncture and blood processing
- The ability to multi-task in fast paced environment
- The ability to work effectively with staff, and other internal and external sponsor and agencies
- At least one year of clinical laboratory and phlebotomy or equivalent experience
Benefits
- Comprehensive benefits
- Total rewards package
- Annual bonus
- Long-term incentive opportunities
Company overview
Sarah Cannon Research Institute (SCRI) is a premier oncology research organization and global leader in community-based clinical trials. Founded in 2004 through a joint venture between Tennessee Oncology and Hospital Corporation of America, SCRI has established itself as one of the world's leading cancer research institutions. With headquarters in Nashville, Tennessee, the institute operates across more than 200 locations in over 20 U.S. states and the United Kingdom, bringing together more than 1,300 research physicians. SCRI specializes in conducting first-in-human clinical trials, having completed over 850 such studies since its inception, and has contributed significantly to the development of approximately 10 FDA-approved cancer therapies since 1999. The organization focuses primarily on oncology research while also expanding into cardiology, gastroenterology, and other therapeutic areas. SCRI's unique community-based model enables patients to access cutting-edge clinical trials close to home, bridging the gap between academic research centers and local healthcare providers. The institute employs 501-1,000 professionals and maintains strategic partnerships with pharmaceutical and biotechnology companies to advance cancer treatment innovations.