Work Schedule
Second Shift (Afternoons)
Environmental Conditions
Office
Job Description
Responsible for the bioinformatics programming aspects of clinical trials from design through analysis and reportingActs as a key contact for client interactions and bid defenses or internal contact for large technical initiatives and ensures effective delivery across all project requirements including communicating priorities and work direction to complete assigned tasks on time and within budget Oversees the resourcing of studies or technical initiatives and develops programming strategies and timelines to ensure process and programming efficiencies Essential Functions and Other Job Information Essential Functions Reviews and ensures adherence to departmental working practice documents and SOPs and contributes to their development Works to increase the visibility of the company by encouraging and actively contributing to the publications of articles in industry journals and presentations at conferences including contributions to indsutry advancements in clinical trial computation methods Monitors and ensures adherence to contractual obligations or limits with our clients Works directly with project team leaders and client representatives to assess and develop project goals and timelines May serve in a project lead role on selected multiple projects including NDAs complex programs tool development and acting as a reviewers of key submission materials for regulatory authorities or deployment of tools processes May lead Investigations into technical issues related to SAS data collection platforms eg Medidata and the computational platforms used within the department Acts as a subject matter expert in leading or assisting efforts to conduct clinical trial statistical analysis May manage computational environments by identifying resource and equipment requirements conducting effective capacity planning and managing software and hardware availability Provides general infrastructure