Senior Programmer Submission

Overview As an experienced programmer, you will hold a combined project leadership and hands-on technical statistics role. Working across a defined area within the sponsor team you will be leading studies and working on sponsor systems. Responsibilities Employees may be required to perform some or all of the following: · Program and validate datasets and SDTMs, including complex efficacy, labs, etc. · Program complex non efficacy outputs/ figures · Perform Senior Review and Deliver QC of non- statistical output · Develop and debug complex macros · Become involved in developing the standard macro library and take responsibility to implement standard macros within a study · Create, QC and update complex dataset specifications (including efficacy) for single/ multiple studies, ISS/ISEs, etc · Review more complex study design SAP without supervision · Review all shells without supervision and provide feedback · Knowledge, interpretation and implementation of current SDTM, ADAM standards · Knowledge of FDA CRT requirements including define.xml and define.pdf · Lead team and be responsible for creation of CRT packages · Become familiar with and follow study documentation · Lead a team for furthering programming development · Ensure the principles in the PHASTAR checklist are followed rigorously · Archive study documentation following instructions in supplied SOPs · Act as a Lead programmer on multiple studies under same project, ensuring quality and timely delivery · Liaise with St