Associate Director Biostatistics

Employer
CSL Behring
Location
King of Prussia, Pennsylvania
Posted
Aug 31, 2020
Ref
R-118162
Hotbed
Pharm Country
Required Education
Masters Degree/MBA
Position Type
Full time
About CSL

With operations in 35+ nations and ~ 22,000 employees worldwide, CSL is driven to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment.

CSL is the parent company of CSL Behring and Seqirus. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. CSL Behring operates CSL Plasma , one of the world's largest collectors of human plasma, which is used to create CSL's therapies. Seqirus is the second largest influenza vaccine company in the world and is a transcontinental partner in pandemic preparedness and a major contributor to the prevention and control of influenza globally.

We invite you to take a look at the many career possibilities available around the globe and consider building your promising future at CSL by becoming a member of our team!

Job Description

• Statistician: Provides statistical thought partnership and sample size calculations for study design and CDPs, including Go-No Go criteria and PTS calculations
• Responsible for project-wide planning of analyses
• Responsible for quality and timely delivery of interim and final results, including integrated analyses for submissions
• Designs and oversees execution of observational studies such as PASS, natural history, etc.
• Accountable for epidemiologic evidence generation in support of clinical development plans, safety signal evaluations and regulatory submissions
• Prepare abstracts, posters, oral presentations and written reports to effectively communicate results of clinical programs and studies to internal and external stakeholders and colleagues with varying levels of clinical research knowledge.
• M.S. or PhD in Statistics, Epidemiology or related field. For statistical programmer: Bachelor's or above. • At least 8-10 years of industry experience, of which at least 5 years in biotech/pharma • Demonstrated use of innovative / creative methodology for transformation and analysis of clinical or epidemiologic/real world data • May manage a small team of people