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Senior Statistical Programmer Statistics & Data Corporation (SDC). . SDC is a team of diversified professionals who deliver exceptional Biometric Services, Consulting, and Technology Solutions to pharmaceutical, biologic, and medical device/diagnostic companies. Since 2005 our purpose has been to partner with sponsors to provide high quality and experienced team members to develop great medicines that save lives and cure diseases in the most efficient manner possible. Our global team operates as a value partner to our clients by fulfilling their needs as our own and delivering exceptional results. We are a specialty CRO in that we provide scalable service offerings, focused services area specialists, efficient project timelines, optimal technology solutions, and proven success and experience. Our commitment to our clients is the same commitment to our employees. By offering strong benefits including competitive pay, generous time off, attainable career advances, positive work/life balance and 401k matching (US), we are able to attract some of the most talented people in the industry. . This person will provide statistical programming support to clinical trials. Produce statistical analyses, including generating analysis datasets, tables, listings, and figures for clinical trials. Create SDTM mapping and datasets. Develop and maintain the infrastructure for project files of SAS datasets and SAS code. Support Data Management in data set creations/transfers, integrity checks, and quality audits. Act as a liaison between clinical and subcommittees and project teams on an as-needed basis.. ***Candidates must reside in Arizona or along the east costal line in US***. Recruiting agencies, please do not submit unsolicited referrals for this or any open role. We have established agency partnerships, and we will not pay any fee associated with unsolicited referrals.. . #LI-Remote. Primary Responsibilities. . Perform all statistical programming required for clinical trial analysis and reporting . . Apply appropriate statistical methods for data analysis and provide statistical programming expertise for project teams . . Review the Statistical Analysis Plan in preparation for programming the planned analyses . . Design/develop SAS macros and other utilities to expedite SAS programming activities . . Generate tables, listings, and figures per protocol, Statistical Analysis Plan, and/or approved client request . . Participate in statistical program validation and quality control activities . . Develop SDTM aCRF and specifications; complete programming and validation of CDISC SDTM and ADaM datasets . . Review ADaM specification documents and ensure the specifications meet the analysis criteria specified in the SAP . . Review pinnacle 21 reports and ensure compliance with CDISC and FDA guidelines . . Develop define.xml, study data reviewer’s guide and analysis datasets reviewer’s guide . . Actively participate in study team meetings . . Interact with other departments, such as Clinical Operations, Project Management, and Data Management to ensure a high level of client satisfaction through successful execution of projects . . Participate in review process of study documents such as the CRF, edit check specifications, and database design specifications written by Data Management . . Program data cleaning checks, as necessary, to assist Data Management’s data cleaning activities . . Participate in installation/validation of statistical software packages throughout the software development lifecycle . . Develop and maintain the infrastructure for project files of SAS datasets and SAS code . . Mentor junior level statistical programmers  Ensure all programming activities and processes performed are conducted according to SDC’s standard procedures and/or sponsor requirements. . Requirements. . Strong analytical skills, with the ability to process scientific and medical data . . Very strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat and SAS Macros . . Basic understanding of SAS/Graph . . Strong problem-solving skills . . Able to work independently . . Excellent knowledge of statistical programming . . Proficient in manipulating and analyzing SAS data  Ability to identify data issues, present problems, and implement solutions . . Capability of communicating technical concepts clearly, concisely, and understandably to non-statistical colleagues . . Good organizational and time management skills, with the ability to multi-task . . Familiarity with clinical trial design and analysis activities and basic knowledge of regulatory guidelines (FDA/CFR, ICH/GCP) . . Understanding of CDISC SDTM and ADaM data models . . Strong interpersonal communication and presentation skills. . Benefits. What you can expect from us:. . We are committed to developing our employees. We recognize achievements, provide growth opportunities and career advancement, and offer a flexible work schedule, engaging work culture, and employee benefits.. . We are passionate about our company culture. Our recognition program is directly tied to our core values of Energy, Integrity, Engagement, Innovation, Ownership, and Commitment.. . We strive to provide a place of belonging to our employees with fun and engaging activities from SDC’s culture club.. . We constantly grow and innovate to support our clients and employees' needs. Global in nature, we bring diverse perspectives enabling our growth in this ever-evolving industry.. . With a proven track record, SDC has successfully executed client clinical programs since 2005.. . Health Care Plan (Medical, Dental & Vision). . Retirement Plan (401k). . Life Insurance (Basic, Voluntary & AD&D). . Paid Time Off (Vacation, Sick & Public Holidays). . Family Leave (Maternity, Paternity). . Short-Term & Long-Term Disability. . Training & Development. . Work From Home. . Profit based incentive. . .