*Hi * *Please find below details for the position of SAS Programmer send me your updated resume.*
*Position: SAS Programmer Analyst* *Location: Cambridge, MA* *Duration 6+ month * *Interview: Phone Interview/Hire* * Summary: The position is responsible for leading clinical programming activities in one or more regions or therapeutic areas. Ensure adequate oversight to outsourced activities by performing quality control steps. Essential Duties and Responsibilities: 1) Lead or contribute to the design, creation and lifecycle management of data collection, validation, analysis and/or reporting systems/software programs (e.g. SAS). For outsourced studies provide oversight to these activities. 2) Lead clinical data standards development and governance activities (e.g. Implementation of CDISC data models like SDTMs, ADaMs, define.xml, LAB, ODM, etc.) and apply/oversee the application of the CDISC data models during the clinical and statistical programming activities. 3) Review relevant DMP sections, CRF design/specifications, SAP and Mock-up tables to provide input from CDISC/Programming perspectives. 4) Develop specifications for multiple data transfers and manage/oversee the actual Data Transfers. 5) _Check the content and format of CDISC submission packages for completeness and compliance with internal and regulatory standards. 6) Assist in the development of resourcing plans and support the training and development of colleagues (e.g. junior Programmers). 7) Manage partnerships with CROs in order to support business goals and proactively address operational issues related to clinical systems or programming.. * * Qualifications:* * • SAS programming expertise • Excellent analytical, problem-solving, organizational, time-management, interpersonal and communication skills • Ability to work on multidisciplinary team and to prioritize activities. • Knowledge of all aspects of the clinical trials process from pre-clinical to post-marketing phases • Ability to interpret and apply regulatory requirements • Knowledgeable concerning all aspects of qualification and compliance assessments • Demonstrated ability to effectively manage relationships with CROs • Experience/Exposure to exercising quality oversight. • Technical understanding of clinical research technologies and software development methodologies • Experience in systems integration and the application of data interchange standards (e.g. CDISC) • Proficient in the use of one or more of the leading Clinical Database Management Systems and clinical/statistical programming environments • Experience supporting continuous process improvement initiatives with a proven track record of success as measured by return on investment • Current with industry developments and trends Education and/or Experience: 2+ years / 4+ years of clinical systems or programming experience in the Pharmaceutical, Device or Biotech industries (Sponsor, CRO or combination) in roles of increasing responsibility. Bachelor’s degree required. Master's degree preferred* Thanks and have a great day *Ranjeet Kumar* *Technical Recruiter* *Srimatrix Inc.* *Phone No. 469.320.9415* *Email: rku...@srimatrix.com <rku...@srimatrix.com>* -- You received this message because you are subscribed to the Google Groups "Open Source Erp & Crm" group. To unsubscribe from this group and stop receiving emails from it, send an email to open-source-erp-crm+unsubscr...@googlegroups.com. To post to this group, send email to firstname.lastname@example.org. Visit this group at https://groups.google.com/group/open-source-erp-crm. For more options, visit https://groups.google.com/d/optout.