Principal Biostatistician FSP

Cytel; Elche; Presencial; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

A leading company in pharmaceutical manufacturing seeks an experienced Principal Biostatistician to lead clinical studies. This role involves providing statistical support, mentoring junior staff, and collaborating on innovative methodologies, contributing to the next generation of patient treatments in a dynamic environment.

Formación

• 9+ years supporting clinical trials in the pharmaceutical or biotechnology industry.
• Ability to work independently and provide innovative leadership.
• Proficiency in SAS programming, with knowledge of R and Python.

Responsabilidades

• Provide statistical support for clinical trials and analyze data.
• Collaborate with teams to implement statistical methodologies.
• Ensure quality and integrity of statistical analyses.

Conocimientos

Leadership

Collaboration

Communication

Attention to Detail

Educación

Master’s degree in statistics or related discipline

Ph.D. strongly preferred

Herramientas

SAS

R

Python

Descripción del empleo

An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, will lead Phase I-IV clinical studies across your region. You are excited and enthusiastic, motivate your teams to do great work, and collaborate easily with your clients. You never settle for what is, but always push clinical development forward to what it could be. You motivate others to do the same.

Job Description

Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Biostatistician, you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be part of this new program.

Position Overview

Our Principal Biostatisticians provide statistical and development support and influence for the associated client's trials, offering expertise in processes, clinical development plans, concept sheets, and protocols. They may also oversee work supported by other vendors. You will formulate integrated analytical approaches to mine data sources, employ statistical methods, machine learning, and deep learning algorithms to discover actionable insights, and automate processes to reduce effort and time for repeated use.

Responsibilities

As a Principal Biostatistician, your responsibilities will include:

• Providing statistical support for clinical trials, including designing and analyzing data, and contributing to development strategies.
• Collaborating with cross-functional teams to develop and implement innovative statistical methodologies.
• Ensuring the quality and integrity of statistical analyses and reports.
• Mentoring junior staff and leading statistical aspects of project teams.

Qualifications

To be successful in this position, you will have:

• Master’s degree in statistics or a related discipline; Ph.D. strongly preferred.
• 9+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry.
• Ability to work independently, demonstrate initiative, and provide innovative leadership.
• Attention to detail, excellent interpersonal and communication skills, and a collaborative attitude.
• Proficiency in SAS programming for quality control and analysis, with knowledge of R and Python.

Seniority level : Mid-Senior level

Employment type : Full-time

Job function : Research, Analyst, and Information Technology

Industries : Pharmaceutical Manufacturing

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