Principal Biostatistician FSP

Cytel; Castellón de la Plana; Presencial; EUR 60.000 - 80.000; Jornada completa

Descripción de la vacante

A leading company in pharmaceutical manufacturing seeks a Principal Biostatistician to drive clinical development. This role will emphasize innovative statistical methods and collaboration across teams while offering autonomy in a groundbreaking program. Suitable candidates will have significant experience in clinical trials and proficiency in SAS and R programming, among other qualifications.

Formación

• 9+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry.
• Ability to work independently with initiative and flexibility.
• Attention to detail and quality focused.

Responsabilidades

• Lead Phase I-IV clinical studies and provide statistical support.
• Develop automation for analytics and collaborate with global stakeholders.
• Project manage tasks and manage change effectively.

Conocimientos

SAS programming

R programming

Machine learning

Deep learning

Communication skills

Collaborative behaviours

Educación

Master’s degree in statistics or related discipline

Ph.D. strongly desired

Descripción del empleo

An experienced Principal Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you 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 a part of this new program.

Position Overview

Our Principal Biostatisticians provide statistical and development support and influence for the associated client's trials providing expertise into processes, clinical development plans, concept sheets and protocols, as well as potentially providing oversight of work supported by other vendors. You will formulate integrated analytical approaches to mine data sources, employ statistical methods, machine learning & deep learning algorithms to discover actionable insights and automate processes for reducing effort and time for repeated use.

Responsibilities

As a Principal Biostatistician, your responsibilities will include :

• Customer Segmentation & Targeting, Event Prediction, Propensity Modelling, Churn Modelling, Customer Lifetime Value Estimation, Forecasting, Recommender Systems, Marketing Mix Optimization, Price Optimization
• Design, run and analyse A / B and multivariate hypothesis tests aimed at optimizing customer and patient experience. Articulate solutions / recommendations to business users. Work with senior data science team members to present analytical content concisely and effectively.
• Develop automation for repeatedly refreshing analysis and generating insights. Collaborate with globally dispersed internal stakeholders and cross-functional teams to solve critical business problems and deliver successfully on high visibility strategic initiatives.
• Project manage own tasks and work with allied team members; plan proactively, anticipate and actively manage change, set stakeholder expectations as required. Independently identify research articles and reproduce / apply methodology to business problems.

Qualifications

Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have :

• Master’s degree in statistics or a related discipline. Ph.D. strongly desired.
• 9+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry.
• Ability to work independently, demonstrate initiative and flexibility through effective and innovative leadership.
• Attention to detail and quality focused, excellent interpersonal and communication skills, innovative, and collaborative behaviours.
• SAS programming skills for QCing critical outputs, Efficacy / Safety tables, and working closely with Programmers.
• Knowledge of R programming (R Shiny / Python).

Seniority level : Mid-Senior level

Employment type : Full-time

Job function : Research, Analyst, and Information Technology

Industries : Pharmaceutical Manufacturing

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