Associate Director, Biostatistics
Job
CSL
King of Prussia, PA (In Person)
Full-Time
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Job Description
Associate Director, Biostatistics Employer CSL Location King of Prussia, PA Start date Apr 12, 2026 View more categories View less categories Discipline Science/R D , Biostatistics Required Education Masters Degree/MBA Position Type Full time Hotbed Pharm Country , Best Places to Work Apply now Save job Click to add the job to your shortlist You need to sign in or create an account to save a job. Send job Job Details Company Job Details The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions, and is accountable for the statistical deliverables within the program. 1 Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions 2 Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews. Lead statistical strategy for planning and study execution (member of Study Executive Team, Clinical Development Team) and quantitative evaluation to clinical trials, regulatory submissions, and related documents. 3 Provide statistical thought partnership for innovative study design and clinical development plans, including Go-No Go criteria and probability of technical success calculations. 4 Provide for project-wide planning of analyses; quality and timely delivery of interim and final results, including integrated analyses for submissions. 5 Represent Biostatistics in interactions with regulatory authorities (eg, FDA, EMA, PMDA) 6 Be responsible for interpreting analysis results and ensuring reporting accuracy in study reports and regulatory documents. 7 Manage outsourcing operations or work with internal statistical programmers within the responsible program. Ensure timeliness and quality of deliverables by
CRO/FSP. 8
Support or lead improvement initiatives within the department, organization and/or pharma industry. 9 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. QualificationsEducation:
PhD or MS in Biostatistics, Statistics or related field- PhD with 8 years of experience or MS with 11 years of experience in drug development
- Experience providing statistical leadership at compound/indication level
- Demonstrated statistical expertise and leadership in facilitating and optimizing the (pre/early/full
- clinical development strategy
- Solid experience in applications of advanced statistical methodologies
- Leading roles in regulatory submissions
- Experience in interactions with major regulatory authorities preferred
- Experience with CROs (either managing a CRO, or having worked in a CRO) or managing internal deliveries preferred
- Track record of innovation preferred Competencies
- Familiarity with regulatory guidance and interactions
- Broad knowledge of clinical development and processes
- Ability to collaboratively work and provide leadership in matrix environment
- Strong interpersonal and communication skills (verbal and written in English)
- Good working knowledge of SAS and/or R
- Expertise in a range of statistical methodologies
- Demonstrated use of innovative / creative methodology for analysis of clinical data
- Familiarity with relevant regulatory guidance documents
- Expertise in CDISC, statistical programming, and/or data standards About CSL Vifor CSL Vifor is a global partner of choice for pharmaceuticals and innovative, leading therapies in irondeficiency and nephrology.
CSL, CSL
Behring, CSL Seqirus and CSL Vifor visit https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/ . Our Benefits For more information on CSL benefits visit How CSL Supports Your Well-being | CSL . You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more about inclusion and belonging visit https://www.csl.com/careers/inclusion-and-belonging Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement . Company CSL is a global biotechnology company with a dynamic portfolio of lifesaving medicines, including those that treat hemophilia and immune deficiencies, vaccines to prevent influenza, and therapies in iron deficiency and nephrology. Since our start in 1916, we have been driven by our promise to save lives using the latest technologies. Today, CSL- including our three businesses, CSL Behring, CSL Seqirus and CSL Vifor
- provides lifesaving products to patients in more than 100 countries and employs 32,000 people.
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