| Urgent need : Sr. Statistical (SAS) Programmer at 100 % REMOTE at Remote, Remote, USA |
| Email: [email protected] |
| Hi, Please find job description below; VISAS- No-h1b TITLE- Sr. Statistical (SAS) Programmer LOCATION- 100 % REMOTE PST WORKING HOURS DURATION- 12 MONTHS CONTRACT INTERVIEW-TELEPHONIC AND WEBEX We are partnering with the company, , an oncology-focused biotech company in Northern California. They are looking for a Sr. Statistical (SAS) Programmer with experience supporting solid tumor oncology groups. This client has had issues in the past with candidate who have padded resumes, so the vetting process will be thorough with a questionnaire and technical interview prior to meeting with the hiring manager. The Qualifications: 5+ years' experience in statistical programming with clinical data and SAS 3 - 5 years of Oncology experience Strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat and SAS Macros UNIX, S-Plus, CDISC, and SAS/GRAPH experience desirable Ability to communicate verbally and in writing in a clear and timely manner Experience in Biotech/Pharmaceutical industry preferred This person will perform statistical analysis on data related to product development in a research and development environment. Uses statistical software (SAS, R, etc.) to create and maintain listings, tabulations, graphical summaries, and formal statistical estimates and tests. Creates datasets in a standard format (i.e. SDTM), analysis datasets (i.e. ADaM), assesses quality of data analysis programs, and develops automated analysis tools, where appropriate. Develops programs to assist with data review such as edit checks and custom listings. May be responsible for data integration used for clinical summaries and/or creation and quality control of statistical submission components to regulatory agencies. May partner with biostatisticians and clinical data management staff in establishing standards for clinical data collection, management and/or reporting of data The Qualifications: 5+ years' experience in statistical programming with clinical data and SAS 3 - 5 years of Oncology experience Strong SAS programming skills required, with proficiency in SAS/Base, SAS/Stat and SAS Macros UNIX, S-Plus, CDISC, and SAS/GRAPH experience desirable Ability to communicate verbally and in writing in a clear and timely manner Experience in Biotech/Pharmaceutical industry preferred The Education: BS/BA degree in related discipline and seven years of related experience; or, MS/MA degree in related discipline and five years of related experience; or, PhD in related discipline and two years of related experience, or; Equivalent combination of education and experience. Knowledge, Skills and Abilities: Extensive experience in relevant industry/profession and area of specialization. Uses professional concepts and company objectives to resolve complex issues in creative and effective ways. Identifies and implements methods and procedures to achieve results. Leads or manages the work of others by providing guidance to subordinates or teams based on organizational goals and company policy, with responsibility for results, including costs, methods and staffing. Performs a variety of complicated tasks with a wide degree of creativity and latitude. Has complete understanding and wide application of technical principles, theories, concepts and techniques. Has good general knowledge of other related disciplines. Applies strong analytical and business communication skills. Essential Duties and Responsibilities: Independently develops SAS or other programs, and specifications (e.g. SDTM, ADaM), for use in study or other analyses, such Integrated Safety Summaries. Must be able to program defensively, check results, and consistently produce accurate output. Independently verifies other programmers results. Serves as oversight, point-of-contact, and quality control for datasets in SDTM and ADaM format as well as tables, listings, and figures (TLFs) produced by CROs, including clear documentation of the process that was followed in the form of specifications, trackers, and checklists. Adheres to FDA regulations and company policies regarding training records, guidelines, and SOPs. Supports ad-hoc requests as needed. Works on multiple tasks at the same time and prioritize tasks to meet business needs. Trouble-shoots technical and project issues. Helps with the infrastructure development of the department. Assists team to ensure timelines for the study and/or project are met. Assists with training new employees and contractors, in particular on study specifics and departmental programming conventions and standards. Communicates with outside departments and/or CROs. Regards, Vijay Kumar | Lead Recruiter Trail Blazer Consulting LLC | Astoria, NY 11105 Office: 914-650-4600 Ext: 148 Keywords: business analyst active directory rlang microsoft Massachusetts New York |
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| Fri Sep 22 23:25:00 UTC 2023 |