Job Openings at IQVIA

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.

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 Manager for the Biostatistics department, you will provide direction and guidance in carrying out project assignments, interfacing with clients and other internal departments, and applying statistical methods to project work.

With site/staff level of visibility, you will manage a team of Biostatistics staff and provide training, guidance, and mentorship to staff members.

Along, with communicating on project progress, staffing concerns, including resource allocation with the Director, Biostatistics

You will perform expert reviews and participate as senior statistician on major projects, including developing/reviewing protocols, preparing analysis plans, overseeing the conduct of analyses, and preparing integrated clinical and statistical reports.

Requirements:

• BSc or MSc degree in Biostatistics or related field and between 5-7 years’ relevant experience within the life-science industry, along with at least 1-year experience in supervising/managing staff
• Familiarity with most complex statistical methods that apply to Phase I-IV clinical trials
• In-depth knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Familiarity with moderately complex statistical methods that apply to applicable clinical trials
• Strong working knowledge of SAS

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

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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.

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 Biostatistician 2, 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 develop statistical methods sections of protocols and review case report forms (CRFs), coupled with, preparing analysis plans, and writing specifications for analysis files, consistency checks, tables, and figures.

Along with, communicating with clients regarding study protocol or statistical analysis issues as they arise and interpreting analyses and writing statistical sections of study reports.

Acting as a lead on studies, you will train and mentor staff and manage scope of work and budget and provide revenue and resource forecasts for single studies.

Requirements:

• BSc or MSc degree in Biostatistics or related field, and 2-4 years’ relevant experience within the life-science industry
• Familiarity with moderately complex statistical methods that apply to applicable clinical trials
• Good working knowledge of SAS and CDISC
• Ability to effectively manage multiple tasks and projects.

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