Gerente general

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, 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, & deep learning algorithms to discover actionable insights, and automate processes to reduce effort and time for repeated tasks.

Responsibilities

As a Principal Biostatistician, your responsibilities will include:

1. Customer segmentation & targeting, event prediction, propensity modeling, churn modeling, customer lifetime value estimation, forecasting, recommender systems, marketing mix optimization, price optimization.
2. Design, run, and analyze A/B and multivariate hypothesis tests aimed at optimizing customer and patient experience. Articulate solutions and recommendations to business users. Collaborate with senior data science team members to present analytical content clearly and effectively.
3. Develop automation for regularly updating analyses and generating insights. Collaborate with globally dispersed internal stakeholders and cross-functional teams to solve critical business problems and deliver on high-visibility strategic initiatives.
4. Project manage tasks independently, plan proactively, anticipate and manage change, and set stakeholder expectations. Reproduce and apply research methodologies to business problems by reviewing research articles.

Qualifications

At Cytel, we support our employees' success through training, development, and support. To succeed in this role, you will have:

• Master’s degree in statistics or a related discipline; Ph.D. is highly desirable.
• 9+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry.
• Ability to work independently, demonstrate initiative, and lead with innovation and flexibility.
• Attention to detail, quality focus, excellent interpersonal and communication skills, and a collaborative spirit.
• SAS programming skills for quality control, efficacy, and safety tables, and working closely with programmers.
• Knowledge of R programming (including R Shiny) and Python.

Seniority level : Mid-Senior level

Employment type : Full-time

Job function : Research, Analyst, and Information Technology

Industries : Pharmaceutical Manufacturing