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Senior manager biostatistics (m/f/d)

Bad Homburg
Fresenius Kabi
Senior Manager
Inserat online seit: 14 April
Aufgaben der Stelle

Your responsibilities

  • Management, review and evaluation of biostatistical solutions and strategies for pre-clinical and clinical studies (phase 1-4, non-interventional incl. RWE studies) conducted and supported by Fresenius Kabi

  • Biostatistical assurance of quality control for Fresenius Kabi company sponsored trials worldwide, including guidance and oversight of contract research organizations to ensure project timelines and goals

  • Study planning, including study design discussions and sample size calculations

  • Development of statistical analysis plans (SAPs)

  • Conduct of statistical analyses and interpretation of statistical results

  • Contribution to clinical study reports, including integrated summaries for submissions

  • Participate in the development of CRFs, edit check specifications, and data validation plans

  • Contribute to the creation, maintenance, documentation, and validation of standards for programming tools, outputs, and macros

  • Statistical programming for Quality Control of critical outputs

  • Your profile

  • You have a completed university degree in (Bio-) statistics or mathematics or equivalent

  • You have at least 5 years experience in CROs and / or the pharmaceutical/biotechnology industry

  • You enjoy working on challenging scientific projects in an international setting and in multidisciplinary teams

  • You are passionate about clinical development and analysis, comprehensive knowledge of statistical methodology in design and analysis needed for clinical research

  • You are highly motivated to explore and implement AI‑supported methods for practical biostatistical applications and efficiency gains in clinical studies

  • You bring knowledge of Real-World research methodology

  • Experience in PK/PD studies (BE studies) / adaptive designs is a plus

  • Excellent knowledge of SAS is mandatory, knowledge of R programming is a plus

  • You have a solid understanding & implementation of CDISC requirements for regulatory submissions (in particular ADaM)

  • You have strong communication skills to present and explain the methodology and consequences of decisions

  • You are fluent in English (written & spoken)

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