Work Schedule
Second Shift (Afternoons)
Environmental Conditions
Office
Job Description
Responsible for the bioinformatics programming aspects of clinical trials from design through analysis and
reporting.Acts 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 (e.g., 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 productive capacity planning, and managing software
and hardware