Clinical Trials Statistician
Há 6 dias
Company Overview
Mai Fortrea Development Limited is a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas.
Salary
We offer a competitive salary package, comprehensive benefits, and a rewarding bonus structure, estimated to be around $145,000 per annum, based on industry standards and location.
Job Description
As a Senior Biostatistician at Mai Fortrea Development Limited, you will play a crucial role in the design, analysis, and interpretation of clinical trials, directly impacting the development of innovative therapies and treatments. You will work dedicated to a client specializing in the development of top-level clinical trials within a wide variety of therapeutic areas such as diabetology, cardiovascular, oncology, respiratory, neurological, immunology etc.
Your Responsibilities:
- Design and implement statistical strategies for clinical trials within various therapeutic areas.
- Develop statistical analysis plans, ensuring their appropriateness for study objectives.
- Perform statistical programming tasks using SAS for analyses and generate study reports.
- Collaborate with cross-functional study teams to contribute statistical expertise and guidance.
- Provide expertise on statistical methodology, sample size calculations, and innovative trial design.
- Ensure the quality and integrity of statistical deliverables.
Required Skills and Qualifications
You must have a minimum of 5 years of experience as a Biostatistician within a CRO, biotech or pharmaceutical company. You should have a solid understanding of statistical methods commonly used in clinical trials, including advanced concepts. Extensive knowledge of CDISC standards, base SAS, SAS macros, SAS/STAT, SDTMs, ADaM datasets and TFLs is also required. A strong knowledge of regulatory guidelines (e.g., FDA, EMA) and industry standards is essential.
Benefits
We offer a supportive and inclusive working environment that values and appreciates individual contributions. You will have access to a diverse team of research professionals, fostering collaboration and continuous learning. Our flexible work policy allows you to work remotely from anywhere, promoting a healthy work-life balance.
Why Work with Us?
Pioneering Research: Join a CRO at the forefront of clinical trials within multiple therapeutic areas.
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