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IQVIA

Senior Biostatistician - Global BIOS (Permanent Homebased)

Posted Yesterday
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In-Office or Remote
Hiring Remotely in Nairobi
Senior level
In-Office or Remote
Hiring Remotely in Nairobi
Senior level
As a Senior Biostatistician, you'll lead statistical consulting and technical support for clinical trial studies, manage project scope and budgets, and collaborate with medical staff to produce reports.
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Join us on our exciting journey!

The Global Biostatistics (Data Sciences, Safety & Medical) 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.

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.

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.

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. 

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 IQVIA to see where your skills can take you

  • Global exposure

  • Variety of therapeutic areas

  • Collaborative and supportive team environment

  • Access to cutting-edge and innovative, in-house technology

  • Excellent career development and progression opportunities

  • Work-Life Balance, with a strong focus on a positive well-being

Unleash your potential!

It takes passion to make the extraordinary possible for patients. Our culture of innovation and collaboration enables us to explore new possibilities and help improve health around the world.

When you join our diverse, global team, you’ll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

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