Statistical Programmer

DUTIES
•Perform the work of statistical programming services to achieve quality, timely and cost-effective study deliverables
•Prepare datasets for analysis by merging files, creating analysis variables, editing data and developing documentation
•Remain informed of new developments in statistical programming that are relevant to the industry and support to the innovation of new reporting systems
•Support the creation of statistical programming standards that comply with regulatory requirements and increase efficiency and quality across studies
•Contribute to the creation of standard macros and tools in SAS for data analysis and reporting
•Assist with statistical quality assurance review
•Contribute to the design and use of appropriate data collection and quality control methods
•Mentor/train selected Associates
•Perform project in compliance with regulations
•Develop positive relationships with clients/colleagues
•Function at a level that affords respect by team members
•Ensure schedule, budget and quality commitments are met for the client
•Communicate project/team issues
•Handle challenging situations and communicate to project Medical Research Manager
•Contribute to presentations
•Interact as needed with clients/auditors/inspectors/subcontractors/consultants/other individuals or departments
•Participate in meetings with prospective clients
•Provide relevant information to support the creation of proposals
•Offer opportunities to clients for expansion

QUALIFICATIONS
•Bachelor’s degree or equivalent experience and a minimum of 3 years of relevant experience; or Master’s or Doctorate degree in Biostatistics/Statistics/Epidemiology/Applied Math(or similar) or equivalent experience
•Experience with SAS programming projects(pharma/medical device industry)
•Fuency in English+Spanish

COMPETENCIES
•Knowledge/experience with SAS programming
•Ability to organize and manipulate large datasets and to express complex statistical programming concepts and technical information