| Looking for SAS Programmer- 100% remote at Remote, Remote, USA |
| Email: [email protected] |
| From: Vick Singh, PEOPLE FORCE CONSULTING, INC. [email protected] Reply to: [email protected] Role - SAS Programmer 7 - 10 yrs Location - 100% remote(EST work hours) Duration - 12 monthe + Mandatory Skills: Statistical programmer :- (Experience in SAS, experienced in SDTM and creation of Submission Package) (Experience in SAS, experienced in SDTM and creation of Submission Package)' Plan and lead the development of project-related solutions to the full scope of statistical programming tasks. Provide technical expertise to the Statistical Programming department. CRFs, ADaM, SDTM, TLFs are MUST HAVE. RESPONSIBILITIES Perform and plan: (i) the programming, testing, and documentation of programs for use in creating statistical tables, figures and listing, (ii) the programming of analysis dataset (derived datasets) and transfer files for internal and external clients. (iii) the programming quality control checks for the source data and report the data issues periodically. Detect errors in detail,corrects them (e.g., reviews tables/listings, edit checks output and SAS programs to ensure quality of deliverable)and report it to appropriate personals (internal or external clients) Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions toSPteams andStatistical Programming department. Perform and plan the development, implementation and validation of new process technologies, macros and applications. Fulfill project responsibilities at the level of technical team lead for single studies, under supervision. Understand timelines for and milestones affecting their work and alert supervisor to potential slippage. Provide training and mentoring to SPteam members All responsibilities are essential job functions unless noted as nonessential REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Knowledge of statistics, programming and/or clinical drug development process In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Ability to implement programming specifications, as appropriate. Ability to estimate programming scope of work and assist in communicating project status. Working knowledge of Base SAS, SAS/STAT, SAS Graphand SAS Macro Language. = Exhibits routine and occasionally complex problem solving skills. Recognizes when negotiating skills are needed and seeks assistance.. Good organizational, interpersonal, leadership and communication skills. Ability to effectively handle multiple tasks and projects, under supervision. Excellent accuracy and attention to detail Ability to establish and maintain effective working relationships with coworkers, managers and clients MINIMUM REQUIRED EDUCATION AND EXPERIENCE Masters degree in computer science or related field and 1 year relevant experience; Bachelor's degree in computer science or related field |
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| Wed Oct 19 18:08:00 UTC 2022 |