Job Title - Senior Clinical Programmer Career Level - D Introduction to role Are you ready to take on a pivotal role in transforming clinical trials through innovative programming and data visualization? As a Senior Clinical Programmer I, you will be at the forefront of developing and validating complex programs and dashboards for ongoing clinical studies. Your expertise will drive high-quality data analysis and reporting, contributing to cross-functional initiatives with significant impact. This role demands advanced technical skills and industry knowledge, empowering you to independently tackle programming tasks while seeking guidance in complex situations.
Accountabilities Design, develop, implement, and validate complex programs using SAS/Python/R or dashboard applications such as PowerBI/Spotfire.Create and maintain PowerBI dashboard applications with efficiency and quality.Process, analyze, and report clinical trial data for review by clinical study teams.Lead high-complexity projects or initiatives within the clinical programming roadmap.Define and build essential processes and tools for global and study-level analytical solutions.Develop best practices to enhance quality, efficiency, timelines, and effectiveness within the function.Provide technical expertise, cross-training, and support to ensure the performance of developed reports and dashboards.Oversee documentation associated with programming tasks to ensure compliance with standard operating procedures, guidelines, and best practices.Ensure high-quality deliverables from self and other programmers.Identify and communicate risks within assigned studies or projects.Collaborate with various teams including data management, development operations, clinical, biometrics, and other relevant cross-functional teams.Develop and maintain data visualization tools, including requirements gathering, data provisioning, and building dashboards.Create and maintain a catalogue of reports to aid data cleaning and reporting activities.Essential Skills/Experience Bachelor's/Master's degree or equivalent in computer science, life science or statistics.Accomplished programming skills in SAS/Python/R/SQL/Power BI/SpotFire or other dashboard technologies.Intermediate knowledge of clinical development process.Good knowledge of industry standards.Ability to influence relevant stakeholders.Excellent analytical and critical thinking skills, writing, communication skills, and ability to work within a cross-functional team.Ability to work in a global team environment.Technical expertise with data capture, data models, data mining, and visualization techniques.Prior experience and understanding of EDC systems like Medidata Rave / Inform / Veeva and Data Platforms like Saama/Entimice, SAS LSAF etc.Desirable Skills/Experience Excellent collaborative skills and the ability to manage complexity and change in a dynamic environment.Broad knowledge of FDA regulations and GCP/ICH guidelines as related to clinical programming processes.Experience in producing analytical dashboards with Power BI, Spotfire or other Business Intelligence tools.Knowledge on MicroStrategy.Ready to make a difference? Apply now to join our team!
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