United States onlyThe Company
Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health.
We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us.
Meet the team:
The Sr Biostatistician with work with an incredible team of Biostatisticians, Statistical Programmers, Clinical Data Managers, Data Scientists, and Medical Writers. We have a fast-paced environment and are looking for dynamic people that want to work on an amazing life-changing technology.
Where you come in:
- Work on the statistical analysis planning and production activities for clinical studies. Activities include designing studies and endpoints, estimating sample sizes with power analysis, creating/reviewing statistical analysis plans, creating/reviewing tables, figures and listings, interpreting results, and addressing limitations in study design and/or statistical methods.
- Work with a project team of biostatisticians, statistical programmers, and medical writers to ensure the timely and accurate completion of analyses (i.e., tables, figures, listings) for clinical study reports.
- Be the statistical lead for pivotal studies in regulatory submission to regulatory agencies (US and ex-US) for IDEs, 501(k)s, and PMAs, as well as feasibility, registry, and other types of studies.
- Provide review and input on clinical protocols, CRFs, and be responsible for the overall data integrity of the study.
What makes you successful:
- Proficiency in statistics methods, applications, and programming. Knowledge and experience in complex statistical methods will be highly valued.
- Great working knowledge and programming skills of SAS and SQL are required. Knowledge and programming skills of R will be highly valued.
- Strong problem-solving skills, self-motivation and self-learning, and the ability to work either independently or as part of a team.
- Excellent oral and written communication skills, with the ability to clearly and concisely communicate statistical concepts and results to non-statistical stakeholders.
What you'll get:
- A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community.
- A full and comprehensive benefits program.
- Growth opportunities on a global scale.
- Access to career development through in-house learning programs and/or qualified tuition reimbursement.
- An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve.
Travel Required
0 - 5%
Experience and Education
- M.S. in biostatistics, statistics, data science, bioinformatics or related field with 5+ years experience is required.
- Ph.D. in biostatistics, statistics, data science or related field with 2+ years experience is preferred.
- Experience in medical device, pharmaceutical, clinical or biotechnology industry will be highly valued.
Please note: The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.
An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Dexcom’s AAP may be viewed upon request by contacting Talent Acquisition at [email protected].
If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact Dexcom Talent Acquisition at [email protected].
View the OFCCP's Pay Transparency Non Discrimination Provision at this link.
Meritain, an Aetna Company, creates and publishes the Machine-Readable Files on behalf of Dexcom. To link to the Machine-Readable Files, please click on the URL provided: https://health1.meritain.com/app/public/#/one/insurerCode=MERITAIN_I&brandCode=MERITAINOVER/machine-readable-transparency-in-coverage?reportingEntityType=TPA_19874&lock=true
To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles, applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team, Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications.
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