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Senior Biostatistician

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From camaraderie to professional development, working at IQVIA provides unique opportunities to advance your career alongside a group of diverse and talented colleagues.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity, and intellectual courage every step of the way.

We have one of the largest Biostatistics departments within the industry of around 1,100+ staff. Due to continued growth, we are seeking new brave minds to join our team.

Overview

As a Senior Biostatistician, you will join one of the largest, award winning and innovative Biostatistics departments and will be given access to cutting-edge in-house technology, allowing you to work on global projects across a variety of therapeutic areas and thanks to our development opportunities and mentoring at all levels, you will be able to progress your long-term career in the direction you choose. 

You will provide statistical consulting and technical support as it relates to the design, statistical analysis, and regulatory submissions of clinical trial studies. 
Collaborate with medical and programming staff to produce interim reports and final reports, allowing a comprehensive understanding and interpretation of the clinical trial data and outcome.  

Key responsibilities

• Performing protocol development, sample size calculation and CRF’s review’s 
• Acting as a statistical team lead for single, complex studies or groups of studies
• Coordinating the development of statistical analysis plans, table shells, and programming specifications
• Managing scope of work and budget, providing revenue and resource forecasts 
• Consulting on operational, statistical, and therapeutic area topics 
• Preparing proposal text and attend bid defense meetings if needed 
• Acting as a primary point of contact for the study team - communicate with team members regarding execution as it relates to timelines, budget, data quality, and interpretation of results
• Providing expert statistical input and review of deliverables for validation requirements 
• Reviewing of the clinical study report to ensure statistical integrity in the reporting of the results 
• Interpreting analysis and crafting statistical sections of integrated reports
• Providing training and mentoring to team members and department staff

Requirements

• BSc or MSc degree in Biostatistics or related field and between 4 - 6 years’ relevant experience within the life-science industry 
• Familiarity with moderately complex statistical methods that apply to applicable clinical trials
• Strong working knowledge of SAS and CDISC SDTM and ADaM 
• Ability to effectively manage multiple tasks and project, ability to communicate and explain statistics 

What's in it for you?

• Interesting and innovative projects 
• Collaborative and inspirational working environment / atmosphere
• Excellent career development and progression opportunities 
• Work – life balance

How to apply

JOIN US
You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately, improve outcomes for patients.

Whatever your career goals, we are here to ensure you get there! To apply for this position, please click here.