Study coordinator Jobs in Bülach
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Study coordinator • bulach
Senior Biostatistician X3
CSLEMEA, CH, Glattbrugg, CSL Behring
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Stampfli AGGlattbrugg, CHSenior Biostatistician X3
CSLEMEA, CH, Glattbrugg, CSL BehringCSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we’re building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.
Could you be our next Senior Biostatistician? The job is in our King of Prussia, PA, Waltham MA and Zurich Switzerland Office. This is a hybrid position and is onsite three days a week. You will report to the Director of Biostats.
The Senior Biostatistician provides and may lead statistical components of statistical contribution to a clinical development program. The Principal Biostatistician implements the statistical strategies for the clinical trials and regulatory submissions within the program, and is accountable for the statistical deliverables.
Responsibilities:
1. Input to statistical strategy and ensure appropriate statistical methodologies applied to study
design and data analysis for clinical trials and regulatory submissions.
2 Provide statistical support in data collection, data analysis, reporting, and submission
preparation.
3 Be accountable for timely completion and quality of the statistical analysis plan.
4 Support Biostatistics interactions with regulatory authorities (eg FDA, EMA, PMDA)
5 Be responsible for interpreting analysis results and ensuring reporting accuracy.
6 Manage outsourcing operations or work with internal statistical programmers within the
responsible projects. Ensure timeliness and quality of deliverables by CRO/FSP. Conduct
reviews of deliverables to ensure quality.
7 Be accountable for the TFL/CDISC package for study report and regulatory submission.
8 Support improvement initiatives and related standards for infrastructure / process / scientific
consulting
Qualifications:
PhD or MS in Biostatistics, Statistics or related field
Experience PhD or MS with1-2 years of experience in drug
development
Competencies -Advanced knowledge and training in applications of statistical methodologies in the context of clinical development
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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.
To learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor visit and CSL Plasma at .
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