Senior Statistician

Worldwide Clinical Trials; Lugo; Presencial; EUR 45.000 - 65.000; Jornada completa

Descripción de la vacante

A leading global contract research organization is seeking a Senior Biostatistician to lead statistical design and analysis. The role involves managing statistical support for projects, mentoring statisticians, and engaging with external groups. Ideal candidates will have a strong background in clinical research and proficiency in SAS.

Formación

• Hands-on expertise as a project statistician.
• Guiding and mentoring other statisticians.
• Experience in clinical research studies.

Responsabilidades

• Manage statistical support for projects.
• Provide expert consultancy and support.

Conocimientos

Proficiency with computer systems

Numeracy skills

Leadership

Statistical applications

Educación

MSc in Statistics

Herramientas

SAS

Descripción del empleo

Worldwide Clinical Trials (Worldwide) is a leading global contract research organization (CRO) that partners with biotechnology and pharmaceutical companies to develop customized solutions advancing new medications — from discovery to market. With a strong scientific heritage, our focus spans cardiovascular, metabolic, neuroscience, oncology, and rare diseases, enabling us to develop flexible plans and solve problems efficiently for our clients.

Our team comprises over 3,000 professionals across more than 60 countries. We are committed to improving patients' lives through innovative therapies.

What Biostatistics does at Worldwide

The Worldwide Biostatistics team is a diverse and experienced group of professionals who collaborate regularly through meetings and informal discussions to address various topics.

The Senior Biostatistician will serve as the lead statistician, developing statistical design and analysis policies and providing expert consultancy within the statistics function. As a Lead Biostatistician, you will work directly with sponsors, study teams, programmers, and other stakeholders. Our work often involves smaller biotech companies lacking internal statisticians, offering opportunities to influence protocol design, statistical analysis, and engage with external groups such as DMCs and regulatory agencies.

What you will do

1. Manage statistical support for one or more projects or sponsor programs, ensuring expert and timely consultancy and support.

What you will bring to the role

1. Proficiency with computer systems and numeracy skills, with the ability to adapt to various software platforms.
2. Hands-on expertise as a project statistician, providing leadership in clinical research projects.
3. Broad experience in statistical applications across all phases (I-IV) of clinical research, with thorough knowledge of regulatory standards, SAS, and other relevant software.

Your experience

1. Minimum of an MSc in Statistics or related field.
2. Experience in guiding and mentoring other statisticians.
3. Previous leadership experience in clinical research studies as a statistician.

J-18808-Ljbffr