The PositionA healthier future. It's what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That's what makes us Roche.
As a Lab Scientist Professional, you participate in scientific studies and activities supporting registrational and non-registrational clinical trials. You will work with a holistic approach to produce vital laboratory test outcomes, applying your excellent attention to detail in a flexible and dynamic team environment.
The Opportunity
You perform high complexity laboratory testing on clinical specimens, and you evaluate quality control and test results against acceptance criteria to support project decisions.
You support the laboratory’s participation as a Clinical Testing Site by performing Clinical Validation testing and accurately completing all applicable documentation.
You comply with study protocols, IRBs, Manuals of Operations, Test Instructions, and related Code of Federal Regulations and ICH guidelines.
You use technical writing skills and Good Documentation Practices to complete project documentation, and you assume accountability for recording methods and results timely and accurately.
You participate in routine lab maintenance, lab safety, ISO, and QSR implementation, and you perform work according to internal safety guidelines and external regulatory agencies such as OSHA.
You support aspects of panel build and sample processing projects, adhering to standards to produce Test Panels and Sample Sets for Clinical Validation Studies.
You analyze alternative approaches to solve problems, and you keep your supervisor informed of project status and critical problem areas.
Who you are
You hold a Bachelor’s degree in Biological/Life Sciences, Chemistry, Biochemistry or a related field, or you have an equivalent combination of education and work experience.
You possess a minimum of 2 years of basic laboratory experience in either an academic or industry setting.
You have experience documenting detailed Clinical Trial activities in Case Report Forms, Sample Accountability, and Investigational Material Accountability Logs.
You know and effectively use the broad concepts of your specialization to resolve problems, and you plan and execute your own work under general supervision.
You demonstrate the ability to multi-task, and you establish and work effectively with individuals or teams outside of your immediate functional area.
Preferred
You have 1 year of preferred relevant industry experience, including experience participating in clinical research work within a laboratory.
You are capable of performing basic troubleshooting for issues related to instrumentation.
You are available for domestic travel approximately 10% of the time.
Relocation benefits are not available for this posting
The expected salary range for this position based on the primary location of Tucson, AZ is 65 500,00 - 121 600,00 USD Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
