Senior Biostatistician

beBeeBiostatician; Madrid; Híbrido; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company in Comunidad de Madrid is seeking a skilled statistician to lead clinical trial design and ensure scientifically robust trials. The ideal candidate will have a PhD in Statistics or Biostatistics and experience with SAS, R, or Python. Responsibilities include designing trial protocols, overseeing study execution, and ensuring compliance. This position offers a hybrid work model and the chance to make a tangible impact on medicine.

Servicios

Work with a top-tier pharmaceutical company

Collaborative science-driven culture

Opportunity to influence projects across development lifecycle

Formación

• Hands-on experience with statistical programming languages like SAS, R, or Python.
• Solid understanding of regulatory frameworks; experience with HTA is a plus.
• Experience in rare disease trials is highly desirable.

Responsabilidades

• Design and implement clinical trial protocols and reports.
• Contribute statistical expertise for regulatory submissions.
• Ensure compliance and quality across multiple studies.

Conocimientos

SAS

R

Python

Statistical analyses

Leadership

Educación

PhD in Statistics or Biostatistics

Descripción del empleo

Overview

Statistician Leadership Position

We are seeking a skilled statistician to lead clinical trial design, ensure trials are efficient and scientifically robust.

The ideal candidate will have hands-on experience with SAS, R, or Python programming languages.

Key Responsibilities

• Design and Implement Clinical Trials : Collaborate with cross-functional teams to develop trial protocols, SAPs, CSRs, and publications
• Provide Statistical Expertise : Contribute to regulatory submissions, market access initiatives, and health authority responses
• Oversee Study Execution : Ensure consistency, compliance, and quality across multiple studies within a therapeutic area
• Maintain Vendor Relationships : Foster strong working relationships with CROs, vendors, and alliance partners
• Drive Strategic Insights : Apply statistical methodology to real-world evidence and contribute to business growth
• Support Audit and Regulatory Processes : Ensure deliverables are audit-ready and compliant with internal SOPs

Requirements

• PhD in Statistics or Biostatistics
• Advanced Statistical Analyses : Design and implement analyses across all clinical phases
• Regulatory Framework Understanding : Solid understanding of regulatory frameworks; experience with HTA is a plus
• Rare Disease Trials Experience : Highly desirable
• Collaborative Mindset : Excellent communication and leadership skills
• Leadership and Mentoring Skills : Ability to lead, mentor, and guide junior statisticians and cross-functional teams

Benefits

• Work with a Top-Tier Pharmaceutical Company
• Collaborative Science-Driven Culture
• Influence Projects Across Development Lifecycle
• Hybrid Work Model
• Make a Tangible Impact on Medicine