Clinical Research Biostatistician/Data Scientist III, Medicine Administration

About this role

• **A Brief Overview** Perform advanced-level statistical analysis at all phases of a research project, from protocol development and study design through data analysis and writing up and reporting results **What You Will Do** * Evaluate research studies, recommend statistical procedures, and prepare statistical plans independently, including, but not limited to, hypothesis tests, regression models, meta-analysis and survival analysis to analyze the data.
• * Prepare comprehensive statistical reports to communicate findings with investigators.
• Prepare statistical components of presentations, abstracts, study protocols, and manuscripts.
• * Describe statistical methods and results to fellow biostatisticians/methodologists as well as to broader audiences with less statistical expertise such as research faculty and staff.
• * Program and create datasets using SAS, R, SQL or Python; combine multiple raw data sets, execute data cleaning and quality control procedures, and derive analytic variables as a data scientist.
• Perform complex programming using advanced options in SAS procedures and macros, or R/SQL/Python features * Serve on institutional committees such as the DSMB (Data Safety Monitoring Board), and create and present biostatistics education sessions * Lead and supervise team of biostatisticians and data scientists and manage assigned projects.
• Mentor and train junior staff, including delegating assignments and providing project guidance as needed * Provide expertise and guidance to investigators at all phases of the research process, from protocol development to study design, dataset analysis, interpretation and publication of results.
• **Additional Responsibilities** * Learn new statistical methods independently as needed.
• * Performs other duties as assigned.
• * Complies with all policies and standards.
• * For specific duties and responsibilities, refer to documentation provided by the department during orientation.
• * Must abide by all requirements to safely and securely maintain Protected Health Information (PHI) for our patients.
• Annual training, the UH Code of Conduct and UH policies and procedures are in place to address appropriate use of PHI in the workplace.
• **Education** * Master's Degree in a research or related field involving statistical analyses (Required) or * Doctorate Degree (Required) **Work Experience** * 5+ years experience in research and statistical analysis (Required) and * Record of successful publication history (Required) **Knowledge, Skills, & Abilities** * Ability to prioritize the work of multiple projects.
• * Experience in a team setting.
• (Preferred proficiency) * Knowledge of GCP and FDA guidelines.
• * Demonstrate ability to multi-task independently and manage time effectively.
• * Ability to understand and communicate statistical analyses and results to others.
• * Computer and programming skills: Word, Excel, and a statistical programming language such as SAS, R, Python or SQL.
• **Licenses and Certifications** * Certification in Human Subjects Protection (CITI) (Required Upon Hire) **Physical Demands** * Standing Occasionally * Walking Occasionally * Sitting Constantly * Lifting Rarely up to 20 lbs * Carrying Rarely up to 20 lbs * Pushing Rarely up to 20 lbs * Pulling Rarely up to 20 lbs * Climbing Rarely up to 20 lbs * Balancing Rarely * Stooping Rarely * Kneeling Rarely * Crouching Rarely * Crawling Rarely * Reaching Rarely * Handling Occasionally * Grasping Occasionally * Feeling Rarely * Talking Constantly * Hearing Constantly * Repetitive Motions Frequently * Eye/Hand/Foot Coordination Frequently **Travel Requirements** * 10%

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