Oncology Clinical Lab Technician

McKesson Corporation; Orlando (FL); On-site; USD 42,000 - 56,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Lab Technician to perform high-level medical laboratory processing for samples from clinical trials. You will implement improvements to enhance lab efficiency and ensure precise processing and shipping of PK/PD samples per study sponsor instructions.

You will work closely with study sponsors and research staff, maintaining accurate logs, EMR documentation, and sample records while scheduling couriers and ensuring dry ice

Qualifications

• Vocational or technical training in laboratory processes and/or phlebotomy.
• Current BLS certification required.
• 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 external sponsor teams.

Responsibilities

• Initiate improvements, tools, processes and forms to enhance lab efficiency and quality.
• Process and ship pharmacokinetic/pharmacodynamic samples per sponsor instructions.
• Serve as primary processor and trainer for specified procedures.
• Attend lab portions of site initiation visits when possible.
• Assist in understanding the lab manual when required.
• Prepare study supplies and source documents for lab sample collection.

Skills

Attention to detail

Multi-tasking

Team collaboration

Communication skills

Education

Vocational or technical training in laboratory process and/or phlebotomy

BLS certification

OSHA knowledge

Tools

EMR systems knowledge

Job description

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, seeks a Lab Technician to perform high-level medical laboratory processing for samples from clinical trials. You will implement improvements to enhance lab efficiency and ensure precise processing and shipping of PK/PD samples per study sponsor instructions.

You will work closely with study sponsors and research staff, maintaining accurate logs, EMR documentation, and sample records while scheduling couriers and ensuring dry ice