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 Sr. Level Clinical Trials SAS Programmer - Direct Hire!

Details
Country: USA
Location: Arizona-Phoenix Tempe, AZ 85280
Total applied: 40
Sr. Level Clinical Trials SAS Programmer - Direct Hire!

Kelly Scientific Resources (KSR), a division of Kelly Services, is recognized as a leader in the staffing industry, with temp, temp-to-hire, and direct hire opportunities at a variety of companies. To satisfy our clients' needs, we work with the best people in the scientific community. That's where you come in. KSR is currently seeking a Clinical Trials SAS Programmer to work for our client in Tempe, AZ. This is a DIRECT hire position and a great opportunity to work in a professional, goal-driven, team-oriented environment. Job Summary:Provide statistical programming support to clinical trials for regulatory submission. Support Data Management in data set creations/transfers, integrity checks, and quality audits. Support Biostatistics in statistical analysis, including generating data listing, tables, and figures for clinical trials. Develop and maintain the infrastructure for project files of SAS datasets and SAS codes. Act as a liaison between clinical and subcommittees and project teams on an as-needed basis.Primary Responsibilities:' Perform or oversee team in performing all SAS programming required for clinical trial analysis and reporting.' Provide statistical programming expertise for project teams.' Actively participate in developing the Statistical Analysis Plan.' Design/develop SAS macros and other utilities to expedite SAS programming activities.' Generate tables, listings, and graphs per protocol, Statistical Analysis Plan, and/or approved client request.' Participate in statistical program validation and quality control activities.' 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 specifications written by Data Management, and Statistical Analysis Plans.' Program data cleaning checks, as necessary, to facilitate 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 codes.' Mentor entry level statistical programmers. ' Ensure all programming activities and processes performed are conducted according to the company's standard procedures and/or sponsor requirements.' Adhere to all aspects of the company's quality system.' Comply with the company's data integrity & business ethics requirements.' Perform other related duties incidental to the work described herein.The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This document is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified. Required Skills:' 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). ' Strong interpersonal communication and presentation skills. Education or Equivalent Experience:' Bachelor's degree in computer science, statistics or other related, scientific field and five years of relevant professional experience; or an equivalent combination of relevant education and/or experience. **Out of state candidates willing to relocate are encouraged to apply.If you are interested in this position, apply today by clicking the APPLY ONLINE or APPLY NOW button, or email your resume to 1274@kellyservices.com Kelly Scientific Resources® has grown into a $200 million global business as the scientific business unit of Kelly Services. Our staff of scientists provides scientific staffing to a broad spectrum of industries including: chemical, cosmetics, food science pharmaceutical, biomedical, consumer products, environmental, medical device, clinical, petrochemical, and clinical research. Kelly provides an incredible opportunity to job seekers all over the globe. We invite you to bookmark our Web site and encourage you to review it regularly for new opportunities worldwide: www.kellyscientific.com Kelly Services is an Equal Opportunity Employer. Learn more about company

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