Chief Statistical Programmer (Oncology)

SDC is a team of diverse professionals providing exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005, our mission has been to partner with sponsors to provide a high-quality, experienced team to develop efficient life-saving and disease-curing medicines. Our global team works as a valued partner to our clients, treating their needs as our own and delivering exceptional results. We are a specialty CRO providing scalable service offerings, specialist services, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients reflects our commitment to our employees. Offering strong benefits including competitive pay, generous time off, achievable career advancements, positive work/life balance, and 401k matching (US), we attract some of the industry's most talented individuals. This job role involves providing statistical programming support to clinical trials, including generating/validating analysis datasets, tables, listings, and figures for clinical trials. Responsibilities also include creating SDTM mapping and datasets, developing and maintaining the infrastructure for SAS datasets and SAS code project files, supporting Data Management in dataset creation/transfers, integrity checks, and quality audits, and acting as a liaison between clinical and subcommittees and project teams on a needed basis. Applicants must live in Arizona or along the east coast of the US. Please note, recruitment agencies should not submit unsolicited referrals for this or any other open role. We have established agency partnerships and will not pay any fee associated with unsolicited referrals. Primary responsibilities include performing all statistical programming required for clinical trial analysis and reporting, applying appropriate statistical methods for data analysis, and providing statistical programming expertise for project teams, among many other specific tasks. Requirements include strong analytical skills, proficiency in SAS programming, excellent knowledge of statistical programming, and familiarity with clinical trial design and analysis activities. Minimum education or equivalent experience required is a bachelor’s degree in computer science, statistics, or another related scientific field with at least eight years of relevant professional experience. We offer benefits such as health care plans (medical, dental & vision), a retirement plan (401k), life insurance, paid time off, family leave, short-term & long-term disability, training & development, work from home, and profit-based incentives.