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50552Mkp - Lead Statistician Clinical Statistics

buscojobs España

Burgos

Híbrido

EUR 60.000 - 80.000

Jornada completa

Hace 4 días
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Descripción de la vacante

A leading company in healthcare is seeking a Lead Statistician to build and lead teams, ensuring appropriate statistical methods in drug development. The role involves collaboration with various stakeholders and the development of innovative methodologies. The ideal candidate will have a PhD or MS in a relevant field and experience in Pharma or Biotech.

Servicios

Work-life balance
Competitive salary
Life insurance
Focus on well-being
Inclusion and diversity programs
Volunteering programs

Formación

  • At least four years of relevant experience in Pharma or Biotech.
  • Experience in team leadership and mentoring.

Responsabilidades

  • Lead statistical efforts for projects within the Statistics Sub-Cluster.
  • Develop and implement innovative statistical methodologies.
  • Influence decision-making in drug development using advanced statistical methods.

Conocimientos

Leadership
Statistical Programming
Fluency in English

Educación

PhD in Biostatistics
MS in Statistics

Herramientas

SAS
R

Descripción del empleo

This offer is part of the Biomedicine and Health Talent Marketplace organized by Barcelona Activa in collaboration with CATALONIA.HEALTH during the Connection Day. BAYER SL is looking for a Lead Statistician Clinical Statistics.

Only candidates who meet the profile requested by the company will be notified. Pre-selected candidates will receive an email from Barcelona Activa confirming attendance and organizational details. Availability for the Job Marketplace is requested for Tuesday, April 29th, from 15h to 18h. Location to be determined.

Functions and Tasks:

BAYER offers a varied and meaningful career in a community of diverse minds, aiming to make a real difference. The mission of Bayer SL is “Health for all, Hunger for none,” delivering breakthrough innovations in healthcare and agriculture.

The Lead Statistician builds and leads teams of statisticians and cross-functional representatives, ensuring the use of appropriate statistical methods during drug development, submission, and lifecycle management, according to global and regional standards, procedures, and regulatory guidelines. They also represent projects to management and governance boards.

Major Tasks and Responsibilities:
  • Lead statistical efforts for projects within the Statistics Sub-Cluster, such as serving as a Project Statistician.
  • Lead virtual teams of statisticians and cross-functional representatives.
  • Contribute to the development and evolution of project standards.
  • Provide statistical and methodological consultation within multidisciplinary teams.
  • Respond to inquiries from health authorities and internal/external partners.
  • Stay updated on regulatory and methodological issues and ensure their implementation.
  • Influence decision-making in drug development and lifecycle management using advanced statistical methodologies.
  • Develop and implement innovative statistical methodologies, collaborating with academic experts if appropriate.
Value Added:
  • Statistics play a crucial role in drug development and lifecycle management, impacting study planning, design, analysis, and reporting to achieve regulatory approval and successful product launch.
  • The Lead Statistician contributes to drug research, development, approval, and lifecycle management, facilitating risk management through innovative statistical approaches.
Work Relations:
  • Early and Global Clinical Leaders
  • Global Safety Leaders
  • Statisticians and Analysts
  • Study and Clinical Team Members
  • Global Regulatory Strategist
  • External statistical experts, software providers, and CROs
Offer:

Work-life balance, competitive salary, financial benefits (e.g., life insurance), and a focus on well-being, inclusion, diversity, and sustainability in a collaborative environment. Social engagement through volunteering programs.

  • Type of contract: Permanent
  • Hours per week: 40h
  • Schedule: 9h to 18h, Hybrid
  • Gross annual remuneration: According to interview and Offices Agreement
Requirements:

PhD or MS in Biostatistics, Statistics, or Mathematics with at least four years of relevant experience in Pharma, Biotech, or similar sectors. Knowledge of clinical drug development, lifecycle management, and related regulations. Experience in team leadership. Embrace VACC behaviors (Visionary, Architect, Catalyst, Coach), mentoring skills, and cultural adaptability. Proficiency in statistical programming (SAS, R). Fluency in English.

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