AD/Director Biostatistics

Skills Alliance

Spain

On-site

EUR 120,000 - 180,000

Full time

46 hours ago
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Job summary

Skills Alliance is seeking an experienced Biostatistics Leader to provide strategic statistical oversight across all stages of clinical development, from early research to late-stage trials. The role partners with cross-functional teams to ensure robust methods and high-quality evidence.

You will lead trial design, adaptive approaches, and advanced modelling, mentor biostatistics professionals, and drive regulatory interactions.

Qualifications

  • Master's or PhD in Biostatistics, Statistics, Mathematics or a related discipline.
  • 10+ years' experience within biotechnology, pharmaceutical or clinical research environments.
  • Proven experience leading statistical strategy across clinical development programmes.
  • Strong expertise in clinical trial design and advanced statistical methodologies.
  • Proficiency in SAS; experience with regulatory submissions is advantageous.

Responsibilities

  • Lead statistical strategy and provide oversight across clinical development programmes.
  • Guide clinical trial design, endpoint selection, sample size calculations and analysis plans.
  • Drive innovative statistical methodologies, including adaptive designs and advanced modelling.
  • Lead, mentor and develop biostatistics professionals.
  • Collaborate with clinical, regulatory and medical teams to support programme delivery.
  • Provide statistical expertise for regulatory submissions, scientific publications and health authority interactions.

Skills

Biostatistics leadership
Trial design
Statistical methodology
Leadership & mentoring
Stakeholder management

Education

Master's or PhD in Biostatistics or related

Tools

SAS
R
Python

Job description

We are seeking an experienced Biostatistics Leader to provide strategic statistical oversight across all stages of clinical development, from early-phase research through to late-stage clinical trials.

This is an exciting opportunity for a senior professional to shape clinical development strategies, lead statistical activities and influence key scientific and regulatory decisions. Working closely with cross-functional teams, you will ensure the delivery of robust statistical methodologies and high-quality clinical evidence.

Key Responsibilities
  • Lead statistical strategy and provide oversight across clinical development programmes.
  • Guide clinical trial design, endpoint selection, sample size calculations and statistical analysis plans.
  • Drive the application of innovative statistical methodologies, including adaptive designs and advanced modelling.
  • Lead, mentor and develop biostatistics professionals.
  • Collaborate with clinical, regulatory and medical teams to support programme delivery.
  • Provide statistical expertise for regulatory submissions, scientific publications and health authority interactions.
About You
  • Master's or PhD in Biostatistics, Statistics, Mathematics or a related discipline.
  • 10+ years' experience within biotechnology, pharmaceutical or clinical research environments.
  • Proven experience leading statistical strategy across clinical development programmes.
  • Strong expertise in clinical trial design and advanced statistical methodologies.
  • Proficiency in statistical software, particularly SAS.
  • Experience supporting regulatory submissions is advantageous.
  • Excellent leadership, communication and stakeholder management skills.
  • Ability to operate effectively within global, cross-functional teams.
  • Fluency in written and spoken English.

This is an excellent opportunity for an established biostatistics professional to take on a strategic leadership position, influence clinical development and contribute to the delivery of high-quality scientific evidence.

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