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Senior Biostatistician - Global BIOS

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Primary Location: Kirkland, Quebec, Canada Additonal Locations: Calgary, Alberta, Canada,CAN; Edmonton, Alberta, Canada,CAN; Mississauga, ON,CAN; Montreal, Quebec, Canada,CAN; Ottawa, Ontario, Canada,CAN; Toronto, Ontario, Canada,CAN; Vancouver, British Columbia, Canada,CAN; Winnipeg, Manitoba, Canada,CAN Full time R1272545

Job description

Join us on our exciting journey!

The Global Biostatistics (Data Sciences, Safety & Regulatory) team at IQVIA are experienced in submissions for all major regions; working together with key groups such as, Global Regulatory Affairs, Safety, Project and Data Management, and Medical Writing, to drive efficiency and accountability.

We have one of the largest Biostatistics departments within the industry of around 1,100+ staff, to which we engage the full range of industry-leading resources and expertise spanning all study phases and therapeutic areas.

Due to continued growth, we are seeking new brave minds to join our award winning and innovative department. You will have the opportunity to work globally and across a variety of therapeutic areas. 

IQVIA Biostatistics helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.

Job Overview:

As a Senior Biostatistician, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas. 

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.

Acting as a statistical team lead for single, complex studies or groups of studies, you will manage the scope of work and budget, providing revenue and resource forecasts, coupled with preparing proposal text and attending bid defense meetings.

You will also 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. 

Requirements:

  • BSc or MSc degree in Biostatistics or related field and between 4 - 6 years’ relevant experience

  • Familiarity with moderately complex statistical methods that apply to applicable clinical trials

  • Good working knowledge of SAS and CDISC SDTM and ADaM

  • Ability to effectively manage multiple tasks and project, ability to communicate and explain statistics

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

What is in it for you?

  • Global exposure

  • Variety of therapeutic areas

  • Collaborative and supportive team environment

  • Access to cutting-edge in-house technology

  • Excellent career development and progression opportunities

  • Work-Life Balance

JOIN US

Embrace your curiosity and grow your career in an exciting environment where development is a priority.

Think boldly and disrupt conventional thinking.

Enjoy what you do.

Whatever your career goals, we are here to ensure you get there!

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. 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. Learn more at https://jobs.iqvia.com

Apply now

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