Associate Director, Biostatistics
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
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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.
Education PhD or MS in Biostatistics, Statistics or related field
Experience -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 iron deficiency and nephrology. We specialize in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision healthcare, aiming to help patients around the world lead better, healthier lives. Headquartered in St. Gallen, Switzerland, CSL Vifor also includes the joint company Vifor Fresenius Medical Care Renal Pharma (with Fresenius Medical Care). The parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people and delivers its lifesaving therapies to people in more than 100 countries.
To learn more about 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.
Perks and Benefits
Health and Wellness
- Health Insurance
- Dental Insurance
- Vision Insurance
- Life Insurance
- Short-Term Disability
- Long-Term Disability
- FSA
- HSA
- Mental Health Benefits
Parental Benefits
- Adoption Leave
- Birth Parent or Maternity Leave
- Non-Birth Parent or Paternity Leave
- Fertility Benefits
- Adoption Assistance Program
- Family Support Resources
Work Flexibility
Office Life and Perks
- Commuter Benefits Program
Vacation and Time Off
- Paid Vacation
- Paid Holidays
- Personal/Sick Days
- Leave of Absence
- Volunteer Time Off
Financial and Retirement
- 401(K) With Company Matching
- Stock Purchase Program
- Financial Counseling
Professional Development
- Tuition Reimbursement
Diversity and Inclusion