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CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we are 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. As Principal Biostatistician, you will provide high level expertise in Research Biostatistics and support research activities in alignment with Therapeutic Area Research Strategies.

Tasks

  • Execute Biostatistics strategies aligned with global therapeutic area and platform priorities, closely collaborating across Global Research with key connections with Bioinformatics & AI, Translational Research, Research Therapeutic area leads and research project teams.
  • Maintain relevant state-of-the-art knowledge and capabilities through literature review and participation in scientific meetings.
  • Oversee statistical design and analysis routines in experiments that translate development strategies into plans to support product development objectives, including process control and validation strategies.
  • Provide statistical input towards experimental designs, statistical analyses, interpretation and reporting of research studies.
  • Provide statistical advice for contacts with regulatory agencies for pre-clinical R&D topics, such as animal ethics applications.
  • Contribute statistical input for regulatory filings for product approvals, on-market support, and scientific publications.
  • Coordinate with other data analysis and computational experts both in house and externally to ensure that CSL R&D is current and compliant in statistical methods.
  • Provide scientific input across R&D programs, including drug discovery, in vitro pharmacology, biomarker development, and OMICS studies.
  • Execute Biostatistical pipelines to enable early decision making across research, drive efficiency and generation of high quality data.
  • Compile scientific reports, regulatory documents, and peer-reviewed publications.
  • Present research findings at internal and external meetings and maintain state-of-the-art knowledge through literature and congress participation.
  • Establish and maintain collaborations with academic institutions, biotech companies, CROs, and other external partners to support execution of the Research Project Portfolio.
  • Support patent filings and legal contract negotiations in collaboration with CSL’s legal and IP departments.

Requirements

  • Postgraduate degree (preferably PhD) in Statistics, Biostatistics, or equivalent experience.
  • Minimum of 5 years of experience in pharmaceutical or biotech R&D, or equivalent experience in a relevant academic environment.
  • Proven experience in working with scientific teams in a global, cross-functional environment.
  • Excellent communication, analytical, and interpersonal skills.
  • Demonstrated ability to drive innovation, manage complex projects, and translate scientific insights into strategic value.
  • High integrity, organizational skills, and a proactive, entrepreneurial mindset.
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Über uns
CSL Behring ist ein biopharmazeutisches Unternehmen, das innovative Therapien auf Basis von Humanplasma und rekombinanten Technologien entwickelt, produziert und vermarktet. Das Unternehmen konzentriert sich auf die Behandlung schwerer und seltener Krankheiten und betreibt Forschung, Entwicklung und Produktion an mehreren internationalen Standorten. CSL Behring ist Teil der global tätigen CSL-Gruppe und liefert seine Produkte weltweit.
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