Associate Director, Biostatistics

Work with cross-functional study/project teams supporting hematology studies and interact with Clinical, Regulatory, Statistical Programming, Data Management and other Research Scientists in reviewing the data, developing and implementing the statistical analysis plan (SAP) for the clinical study report (CSR) and other health authority submission documents. Provides content for manuscripts / presentations and provides statistical support in designing and analyzing clinical trials, and in coordinating the statistical activities for clinical projects.

Essential Duties & Responsibilities:

Develops or assists development of study protocols and SAPs and determines appropriate statistical methodology for data analysis.

Participates in database design meetings to ensure that the data evaluated are in high quality and satisfy analysis requirements.

Collaborates with the statistical programming staff to ensure 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. Applies and implements basic and complex techniques to these analyses under supervision.

Prepares oral and written reports to effectively communicate results of clinical trials to the project team.

Provides responses to queries relating to study design, analysis, and interpretation posed by the clinical monitors, regulatory agencies, and/or investigators.

Involved in research activities for innovative statistical methods and applications in clinical trial development.

? Other Qualifications:

Experiences with clinical trials and knowledge of regulatory guidance are required.

Oncology experience is preferred but not required.

Demonstrated written and oral communication skills and ability to work within a team and work independently are required.

Other important requirements include interdependent/analytic thinking skills, building strategic working relationships, and good decision-making capability.

Education Required:

A minimum of a PhD in Statistics or related field with 4+ years of experience in clinical drug development is required.

Knowledge of SAS and/or R is strongly desirable.

Computer Skills: Knowledge of SAS and/or R is strongly desirable

Travel: Not required

BeOne Global Competencies:

When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

Fosters Teamwork

Provides and Solicits Honest and Actionable Feedback

Self-Awareness

Acts Inclusively

Demonstrates Initiative

Entrepreneurial Mindset

Continuous Learning

Embraces Change

Results-Oriented

Analytical Thinking/Data Analysis

Financial Excellence

Communicates with Clarity

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.