Hi, Hope you are doing great. Please review the below requirement and mail back to *prad...@sriveninfosys.net <prad...@sriveninfosys.net>*
*Title : 3 SAS Clinical Programmers* *Client : PRG* *Duration : 6+ months* *Locations : Multiple – Horsham PA, Raliegh NC & Kansas City KS* *Required Skills:* · Employees at this level are required to perform all tasks associated with a Clinical Programmer and apply a breadth of industry and technical experience and expertise to lead multiple studies and/or integration projects. Additional duties include the following: · Provide leadership and oversight to programs of clinical trials and/or complex clinical trial projects, handling the related technical issues to ensure standard processes are implemented and overall consistency and quality is achieved. Work may include: · Serving as primary functional representative, providing input for clinical programming projects; · Overseeing and coordinating with leads/subleads for the individual trials or components of the project · Mentoring clinical programmers within a project team; · Serving as a resource for, and interacting with, other functional areas to facilitate project timelines; · Integrated database design, documentation and implementation; · Identifying and quantifying changes in scope. · Contribute to interactions with clients and vendors, such as the following: · Bid defense activities · Development and implementation of client/vendor standards · Evaluation of vendors for preferred provider relationships. · Share experience and expertise with internal and external colleagues: · Present department training; · Present at conferences; · Mentor clinical programmers in all clinical programming responsibilities; · Expand and maintain wiki. · Provide input into technical initiatives in order to develop and improve the standard processes within Clinical Programming. Work may include: · Serving as a functional representative, providing input for clinical programming initiatives; Applies knowledge of policies and procedures. Applies knowledge of computerized information systems and standard application software (Windows, MS Office). Excellent written and oral communication. Applies a basic knowledge of Clinical Programming. Applies basic knowledge of programming language, or other software languages/ tools as required. Applies attention to detail. Identifies programming and data issues and seeks guidance on resolution from higher levels. Follows established procedures as outlined in trial specific documents, SOPs and related work instructions. Uses existing techniques to perform accurate and efficient Clinical Programming. Errors can be easily and quickly detected within the immediate work unit and would result in only minor disruption or expense to correct. Close supervision involving detailed instructions and frequent monitoring of work performance. Contacts are primarily within the assigned clinical programming project teams and functional management. Tasks are expected to be learned by peer training, formal training, review of SOPs, related work instructions and trial specific documentation. Follows processes and specifications for the project, clearly communicating questions to Lead CP, mentor or functional management. *Other skills:* · Interact with biostatisticians, pharmacokineticists, medical writers, clinical systems developers, and other operations staff. · Produce figures and documentation of datasets, including define.xml files to support the tabulation and analysis of clinical trials. · Liaise with external data vendors (e.g. central laboratories, ECG vendors) to ensure that data is transmitted in required format. · Apply knowledge of the CDISC Standards, SDTM and ADaM. · Create derived datasets in accordance with derived dataset specifications. · Understand project budgets for clinical programming tasks and communicate potential issues to the project lead and/or functional manager. · Achieve utilization targets. *Thanks & Regards* *Pradeep Kumar* *Technical Recruiter* *Sriven Infosys Inc* *Direct: 718-502-9128* *Email: **prad...@sriveninfosys.net* <prad...@sriveninfosys.net>* | Gtalk: pradeepkumar.sriveninfosys* *URL: *www.sriveninfosys.net -- You received this message because you are subscribed to the Google Groups "REQSRESUMES" group. To unsubscribe from this group and stop receiving emails from it, send an email to reqsresumes+unsubscr...@googlegroups.com. To post to this group, send email to firstname.lastname@example.org. Visit this group at http://groups.google.com/group/reqsresumes. For more options, visit https://groups.google.com/d/optout.