Director Biostatistics

Director, Biostatistics

The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The Associate Director provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and submissions, while partnering closely with Clinical Development and other key stakeholders.

Responsibilities and Accountabilities:

•Define the statistical strategy and ensure appropriate statistical methodologies applied to the clinical development plan, study design and data analysis for clinical trials, and regulatory submissions.

•Provide statistical insight into execution of clinical development, to ensure study conduct leads to a statistically sound and robust data package, maximize probability of program success.

•Interprets analysis results and ensures reporting accuracy in study reports and regulatory documents, abstracts, posters, oral presentations, manuscripts and written reports to effectively communicate results of clinical programs and studies.

•May serve as the point of contact for one or more PSTs within the Therapeutic Area.

•Lead or provide oversight to the analysis delivery and quantitative evaluation of clinical trials, and integrated analysis.

•Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA), which includes leading written responses to regulatory questions and attending regulatory meetings.

Qualifications:

Education

PhD or MS/MA in statistics or related field

Experience

10+ years of experience in clinical development within the pharmaceutical or biotechnology industry

Demonstrated leadership in statistical contributions to clinical programs and regulatory submissions

Experience partnering with cross-functional teams and interacting with health authorities

Experience managing external partners (CROs, consultants)

Competencies

Strong statistical methodology knowledge and clinical trial design expertise

Ability to collaborate and influence across functions and levels

Excellent communication and interpersonal skills

Experience with CDISC standards, programming oversight, and statistical operations

Strategic and analytical mindset with a focus on execution

Ability to work in a matrixed environment and lead through influence

Working Conditions

• This is a hybrid position. Three in-office days per week are required.

Travel Requirements

• Occasional travel to scientific conventions

About CSL Behring

CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. We use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives.

CSL Behring operates one of the world's largest plasma collection networks, CSL Plasma. Our parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people, and delivers its lifesaving therapies to people in more than 100 countries.