Full Time Fraud Data Scientist Jobs in Raleigh, NC

Global Biostatistics

Job Level: Statistical Scientist

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 Statistical Scientist, 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.

With visibility at a team/site/staff level, you will lead complex studies and submissions and develop protocols, review case report forms (CRFs), and develop analysis plans.

You will also provide input or write specifications for tables and analysis files and communicate with clients regarding study protocol or statistical analysis issues as they arise. Along with interpreting analyses and writing statistical sections of study reports.

You will also be accountable for controlling costs and maximizing revenue recognition and running meetings, providing timeline updates and assessing resource needs.

Requirements:

• BS degree with 7 years of experience or MS degree with 5 years of experience OR equivalent experience.
• Strong knowledge of complex statistical methods that apply to applicable clinical trials
• Experience in Early Clinical Development phases with Pharmacokinetic/Pharmacodynamic endpoints preferred
• Strong 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 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 athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

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.