Clinical Research Biostatistician/Data Scientist III, Medicine Administration

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.

Qualifications:
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%