Senior Biostatistician FSP

Cytel • United States,

9d • Onsite

About The Position

An experienced Biostatistician with a passion for clinical development and analysis, adept at utilizing advanced statistical methods, you will support or lead one or more Phase I-IV clinical studies. You are excited and enthusiastic. You 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. 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 Senior 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. Our Senior Biostatisticians perform ad-hoc or exploratory analyses to support submission or Health Authority Questions. Having exposure to regulatory work experience is a bonus, for example, if you understand the regulatory questions and translating them to statistical problems, collaborating effectively, with clinical and regulatory colleagues. Supporting medium complexity clinical trials (starting from Design to Archival experience) and supporting some project-level activities.

Requirements

• Experienced Biostatistician with a passion for clinical development and analysis.
• Adept at utilizing advanced statistical methods.
• Ability to motivate teams to do great work.
• Ability to collaborate easily with clients.
• Ability to push clinical development forward.
• Ability to motivate others.
• Understanding of regulatory questions and translating them to statistical problems.
• Ability to collaborate effectively with clinical and regulatory colleagues.

Nice To Haves

• Exposure to regulatory work experience.

Responsibilities

• Support or lead one or more Phase I-IV clinical studies.
• Perform ad-hoc or exploratory analyses to support submission or Health Authority Questions.
• Support medium complexity clinical trials (starting from Design to Archival experience).
• Support some project-level activities.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: No Education Listed