Develops, coordinates, and provides biostatistical support for related drug/vaccine projects under supervision in Late Development Statistics
Interacts with Clinical, Regulatory, Statistical Programming, Data Management and other our Company's Research Laboratories Scientists in analyzing clinical trials, and in coordinating other statistical activities for clinical drug/vaccine projects under supervision
Shadowing senior statisticians, serves as statistical representative in the cross-functional teams for the clinical trial planning, execution, and reporting
Under supervision of senior statisticians, participates in study design; performs sample size calculations and simulations to support protocol development
Under supervision develops statistical analysis plans and determines appropriate statistical methodology for data analysis
Participates in database design meetings and reviews relevant study documents including CRF, Data Validation Plan, and Medical Monitoring plan to ensure that the data evaluated are in high quality and satisfy analysis requirements
Collaborates with the statistical programming staff to provide definitions, documentations, and reviews derived variables needed for planned analysis; ensures that all programs meet analysis requirements, internal standard operating procedures, and external regulatory requirements
Analyzes data and interprets results from clinical trials to meet objectives of the study protocol
Reviews study results to ensure all the deliveries in high quality
Under supervision of senior statisticians, prepares oral and written reports to effectively communicate results of clinical trials to the project team, management, regulatory agencies, or individual investigators
Involved in research activities for innovative statistical methods and applications in clinical trial development
Requirements
Master’s degree or equivalent in statistics/biostatistics or related discipline
Knowledge of statistical analysis methodologies and experimental design
Familiar with statistical and data processing software e.g. SAS and/or R
Good oral and written communication skills
Able to work effectively with personnel with different functional background
Must also demonstrate the ability to learn, be proactive and motivated, and consistently focus on details and execution
Benefits
medical, dental, vision healthcare and other insurance benefits (for employee and family)