Manager, Biostatistics - Global BIOS
Manager, Biostatistics - Permanent - w / m / d
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.
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.
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?
Variety of therapeutic areas
Collaborative and supportive team environment
Access to cutting-edge in-house technology
Excellent career development and progression opportunities
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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