Roche fosters diversity, equity and inclusion, representing the communities we serve. When dealing with healthcare on a global scale, diversity is an essential ingredient to success. We believe that inclusion is key to understanding people’s varied healthcare needs. Together, we embrace individuality and share a passion for exceptional care. Join Roche, where every voice matters.

A 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.

The Opportunity:

As an integral part of Biometrics Pathology you will Interact with development and clinical investigators to design clinical trials with appropriate statistical methods and adequate sample size for statistical justification of clinical utility claims. This position will write statistical analysis plans as needed to capture design elements and statistical methodology.
A key part of this role performs data analysis and prepares statistical reports of results, quality control (QC) for statistical analyses by other biostatisticians to ensure analysis quality. You will also
troubleshoot and improve current statistical designs, including those developed elsewhere in the organization. You will have the opportunity to maintain expertise in state-of-the-art data manipulation and statistical analyses, and mentors less experienced colleagues.

Who you are:

- You have a Masters with 2-4 years or PhD with 2 years of relevant healthcare experience.
- You have multiple years of experience in FDA submissions 
- You have experience in-vitro diagnostic tests.
- Significant experience in analysis and reporting using statistical software.

Preferred:

 
- Exceptional knowledge of FDA guidelines for in vitro diagnostic devices and the required statistical basis for sensitivity, specificity, agreement rates, and reproducibility testing required for validation and FDA clearance and approval.
- You have a strong ability to collaborate across departments and interact with various levels in the organization.
- You have high attention to detail with skill in producing organized reports 
- You are comfortable writing statistical code and documentation. 
- You are very proficient at SAS or comparable data analysis software.
- Ability to work in a team-focused environment is essential, as all statistical analyses under design control require both lead statistical analysis and quality control (QC), each conducted by different individuals who must coordinate activities.
- You easily manage, prioritize and plan work activities.

The expected salary range for this position based on the primary location of Tucson, AZ is $84,800 and $156,000 annually.  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.

Benefits

Relocation benefits are not available for this job posting.

At Roche, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we’ve become one of the world’s leading research-focused healthcare groups. Our success is built on innovation, curiosity and diversity.

Roche is an equal opportunity employer and strictly prohibits unlawful discrimination based upon an individual’s race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other characteristic protected by law.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.