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Senior Biostatistics Manager (Remote from Germany)

Jobgether

Deutschland

Hybrid

EUR 70.000 - 100.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

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Zusammenfassung

A leading recruitment platform is seeking a highly experienced Senior Biostatistics Manager for a prominent role in Germany, focusing on advanced Real-World Evidence initiatives. This position involves leading complex statistical programs for pharmaceutical and biotech clients, ensuring scientific rigor across study design and analysis. Candidates should possess an advanced degree, strong expertise in SAS, and at least 5 years of experience in a relevant environment. Flexible working arrangements are available, along with opportunities for professional growth and collaboration.

Leistungen

Flexible working arrangements
Opportunity for professional growth
Collaborative environment

Qualifikationen

  • 5+ years of experience as a Lead Biostatistician in a CRO, biotech, or pharmaceutical environment.
  • Proven experience with non-parametric methods, linear and non-linear models, and survival analysis.

Aufgaben

  • Lead complex RWE studies and provide end-to-end statistical oversight.
  • Develop and review Statistical Analysis Plans for regulatory alignment.
  • Contribute to protocol development and author statistical sections.
  • Act as a subject matter expert and present insights at conferences.

Kenntnisse

SAS programming expertise
Statistical Analysis Plans development
Communication of complex statistical concepts
Organizational skills
Attention to detail

Ausbildung

Advanced degree in biostatistics or related field
Doctoral degree preferred

Tools

SDTM datasets
ADaM datasets
Jobbeschreibung

This position is posted by Jobgether on behalf of a partner company. We are currently looking for a Senior Biostatistics Manager in Germany.

This role sits at the center of advanced Real‑World Evidence initiatives, supporting high‑impact studies for leading pharmaceutical and biotech organizations. You will lead complex statistical programs, contribute to post‑market and regulatory strategies, and ensure scientific rigor across study design, analysis, and reporting. Working within a collaborative consulting environment, you will partner closely with cross‑functional teams and senior stakeholders. The position combines hands‑on statistical expertise with strategic leadership and external visibility. Your work will directly influence regulatory decisions and scientific publications. This is an ideal opportunity for an experienced biostatistician looking to shape the future of evidence‑based healthcare.

Accountabilities
  • Lead complex RWE studies and multi-protocol programs, providing end‑to‑end statistical oversight and coordination across teams and locations.
  • Develop and review complex Statistical Analysis Plans, ensuring methodological soundness and regulatory alignment.
  • Perform senior‑level review of Tables, Figures, and Listings prior to client delivery.
  • Contribute to protocol development by authoring statistical sections under senior statistical guidance.
  • Act as a subject matter expert, supporting internal initiatives, procedural documentation, and best practices.
  • Participate in bid defenses, client meetings, and strategic discussions as a statistical lead.
  • Present insights and share knowledge internally and at external scientific conferences and forums.
Requirements
  • Advanced degree in biostatistics, computer science, or a related field; a doctoral degree is strongly preferred.
  • At least 5 years of experience as a Lead Biostatistician within a CRO, biotech, or pharmaceutical environment.
  • Strong programming expertise in SAS, including non‑parametric methods, linear and non‑linear models, categorical data, and survival analysis.
  • Proven experience working with SDTM and ADaM datasets, as well as producing high‑quality Tables, Figures, and Listings.
  • Solid understanding of observational study design, analysis, and reporting processes.Demonstrated ability to clearly communicate complex statistical concepts to technical and non‑technical audiences.
  • Strong organizational skills, attention to detail, and an autonomous yet collaborative working style.
Benefits
  • Opportunity to work on high‑visibility, global Real‑World Evidence projects.
  • Flexible working arrangements, including remote work options.
  • Exposure to international clients, scientific publications, and regulatory‑driven studies.
  • Collaborative consulting environment focused on innovation and scientific excellence.
  • Professional growth through leadership opportunities and knowledge‑sharing platforms.

Why Apply Through Jobgether?

We use an AI‑powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role’s core requirements. Our system identifies the top‑fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team.

We appreciate your interest and wish you the best!

Why Apply Through Jobgether?

Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre‑contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time.

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