Statistical Scientist
About The Position
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 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 projects
- Ability to communicate and explain statistics
Responsibilities
- Lead complex studies and submissions
- Develop protocols
- Review case report forms (CRFs)
- Develop analysis plans
- Provide input or write specifications for tables and analysis files
- Communicate with clients regarding study protocol or statistical analysis issues
- Interpret analyses
- Write statistical sections of study reports
- Accountable for controlling costs and maximizing revenue recognition
- Running meetings
- Providing timeline updates
- Assessing resource needs
Benefits
- 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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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
