Laboratory Technician

McKesson; Orlando (FL); On-site; USD 55,000 - 75,000; Full time

Job summary

McKesson delivers clinical lab services and supports Sarah Cannon Research Institute by performing high-level processing for specimens from patients in clinical trials. The Lab Technician role emphasizes accuracy, documentation, and collaboration with research staff.

Based in Orlando, FL, you will manage PK/PD samples, keep logs, utilize EMR for source documentation, and coordinate courier shipments to ensure timely, compliant processing.

Qualifications

• Vocational or technical training in laboratory processing.
• Current BLS certification.
• Knowledge of OSHA safety requirements.
• Experience with venipuncture and blood processing.
• Ability to multi-task in a fast-paced environment.
• Ability to collaborate with staff and study sponsors.

Responsibilities

• Initiate improvements to tools, processes and forms to boost lab efficiency.
• Process and ship PK and other samples per sponsor instructions.
• Serve as primary processor and trainer for specified procedures.
• Attend the lab portion of the site initiation visit when possible.
• Maintain accurate freezer logs and sample shipping records.
• Use EMR for source documentation.
• Schedule couriers and ensure dry ice supplies.
• Coordinate with nurses to ensure proper lab kits and specimen collection.

Skills

Venipuncture

Lab workflow

EMR documentation

Multi-tasking

Education

Vocational/technical lab training

BLS certification

Tools

EMR systems

Job description

Job Description

As a Lab Technician you will perform high-level medical laboratory processing procedures for specimens received on patients enrolled in clinical trials.

• 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 patients' charts that are accurate and complete. All shipping and processing records should be maintained in the patients' 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

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.

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.

We are an equal opportunity employer and value diversity at our company.

We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.

About McKesson

McKesson delivers careers with purpose and potential. Our focus on better health starts with creating an inclusive environment with strong values where you can build a fulfilling career. We work to distribute medical supplies, bandages, syringes, vials of flu vaccine, and pharmaceutical drugs to help real patients like Jack, an eight-year-old boy battling cancer. We take that job seriously. Together, the work we do is shaping the future of healthcare.