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Senior Biostatistician

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Primary Location: Kirkland, Quebec, Canada Additonal Locations: Mississauga, ON,CAN; Ottawa, ON,CAN Full time R1281796

Job description

Join us on our exciting journey!

The vision of our Real World Evidence teams is to pioneer and lead with scientific and technical expertise, the generation and dissemination of high-quality Real World Evidence that make a true difference to patient lives, globally.  Come join us on this exciting journey!

Our Real World Global Biostatistics & Statistical Programming team delivers insightful analytics for predominantly primary data collection studies, and we are increasingly supporting innovative studies such as External Comparators, Enriched Studies, and Pragmatic Trials.  

We are a highly motivated global team of more than 150 employees, responsible for engaging with our clients early to help shape the statistical analysis in these various study designs; contribute to protocols and deliver results that meet their needs.

We have unique opportunities to define the way our clients develop and apply Real World Evidence for healthcare decision making, so we are looking for the best talent to join us in this effort.

We are collaborative, intellectually curious, entrepreneurial, and constantly looking for opportunities to harness the value of Real World Evidence in an evolving industry!

Job Overview:

As a Senior Biostatistician, you 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.

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

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

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