Vita Global Sciences provides unparalleled professional services in clinical data analytics and functional outsourcing. As an innovator in the Life Sciences space, Vita Global Sciences partners with clients to develop and deliver full service, scalable data solutions in the Pharmaceutical, Biotechnology, Medical Device, & CRO industries. Our growth and success is based largely upon our multi-cultural, and diverse workforce. Our team is our most valuable asset and we allow our team members to grow professionally, as we rapidly grow as a company. We are dedicated to hiring remarkably talented people who are self-directed, determined and smart, often favoring ability over experience. Our work environment provides opportunities to enhance their roles with clear responsibilities and the opportunity to work on a variety of assignments. At VGS, you will have an inspiring trust-based work culture for learning with motivational, approachable and visionary leadership. Working at VGS you will see the impression of an exciting environment to work and grow. Sr. Statistical Programmer I Responsibilities Develop statistical programs in SAS to generate the clinical datasets, tables, listings and figures. Perform validation and QC of the programs, datasets and statistical reports per study requirements. Develop and review CDISC SDTM and ADaM mapping specifications. Responsible for study closeout and providing submission-ready statistical programming deliverables to the client. Ensure compliance of CDISC SDTM and ADaM datasets by running OpenCDISC validator and documenting issues. Generate and review submission documents such as define.xml, SDTM annotated CRF, and reviewers guide. Ensure review of study documents such as Protocol, CRF, and SAP. Communicates effectively within a project team to complete assigned tasks on time and within budget. Effectively implement and promote use of established standards, SOP and best practices. Provide training and mentoring to junior programmers in the team. Requirements Master’s degree or equivalent and relevant formal academic / vocational qualification. 3yrs SAS programming experience. 1yr CDISC implementation experience. Proficient in SAS and Macros and have developed macros to automate functionality. Experience working in Oncology therapeutic area Participated as production or QC programmer at a product and/or study level. Good organizational, interpersonal, leadership and communication skills. Ability to independently manage multiple tasks and projects.