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Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), collaborates with biotechnology and pharmaceutical companies to develop customized solutions that advance new medications — from discovery to approval. 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 of over 3,000 professionals across more than 60 countries is dedicated to improving patients' lives through innovative therapies.
What Biostatistics does at Worldwide
The Biostatistics team is a diverse group of experienced professionals who collaborate regularly through meetings and one-on-one discussions to address various issues.
The Senior Biostatistician will lead statistical design and analysis policies, providing expert consultancy within the statistics function. This role involves working directly with sponsors, study teams, programmers, and external groups such as DMCs and regulatory agencies. Our work often involves smaller biotech companies lacking internal statisticians, offering our statisticians the opportunity to influence protocol design and statistical analysis significantly.
What you will do
* 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
* Proficiency in computer literacy and numeracy, with the ability to adapt to various systems.
* Hands-on experience as a project statistician providing leadership within clinical research.
* Expertise in a broad range of statistical applications across all phases (I to IV) of clinical research, with thorough knowledge of regulatory standards, SAS, and other software.
Your experience
* Minimum MSc in Statistics or related field.
* Experience in guiding and mentoring other statisticians.
* Previous experience leading studies as a Statistician in clinical research.
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