IQVIA
Biostatistician2
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Biostatistician 2 at IQVIA. Skills: Biostatistics, Statistical programming, Data management. Lead biostatistical workstreams. Lead programming workstreams”
What They're Looking For.
Must Have
BSc or MSc in Statistics, Practical experience with real world secondary databases, Practical experience with Finnish national registry data, SAS programming skills, R programming skills, Ability to understand written documentation of Finnish register data, CRO experience, Pharmaceutical industry experience, Communication skills in English, Ability to manage multiple tasks, Deliver high quality outputs within agreed timelines
Nice to Have
MSc in Biostatistics
What You'll Do.
Lead biostatistical workstreams
Lead programming workstreams
Develop statistical methods sections
Prepare statistical analysis plans
Write specifications for analysis files
Write specifications for consistency checks
Write specifications for tables
Write specifications for figures
Contribute to data management
Contribute to statistical programming
Communicate with clients
Provide statistical lead
Deliver with high quality
Deliver within budget
Write Statistical Analysis Plan
Perform QC reviews of SAP
Perform QC reviews of Shells
Write programming specifications
Maintain programming specifications
Assist with protocol development
Assist with sample size calculations
Write statistical programming code
QC statistical programming code
Build customer relationships
Maintain customer relationships
Drive statistical discussions
Provide support for statistical activities
Provide guidance for statistical activities
Provide revenue forecasts
Provide resource forecasts
How You'll Work.
Team & Collaboration
Working with Project Team Lead; Working with supervisor
Communication Scope
Communication skills in English
Process & Methodology
Scope management, Budget management
Full Job Description
As a Biostatistician , you will be given access to cutting-edge in-house technology, allowing you to work on global projects across a variety of therapeutic areas and 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 contribute to/ lead the biostatistical and/or programming workstreams * You will develop statistical methods sections of protocols, prepare statistical analysis plans and write specifications for analysis files, consistency checks, tables, and figures. * You will contribute to data management and statistical programming of Finnish national registry data. * You will communicate with clients regarding study protocol or statistical analysis issues as they arise. * _**Key Responsibilities**_ • provide as a statistical lead in single data-source studies. • Working closely with the Project Team Lead and supervisor to deliver on time, with high quality and within budget. • Writing and performing quality control (QC) reviews of Statistical Analysis Plan (SAP) and Shells. • Writing and maintaining programming specifications. • Assisting with protocol development and sample size calculations. • Writing and/or QCing data management and statistical programming code in R/SAS • Building and maintaining effective customer relationships, driving statistical discussions, providing support and / or guidance for statistical activities. • Managing scope of work and budget, and providing revenue and resource forecasts for single studies • Training and mentoring junior staff. Supporting colleagues and providing motivation as needed. _**Requirements:**_ • BSc or MSc in Statistics/Biostatistics or related field • Practical experience working with real world secondary databases (e.g., national registries, claims, EMR, etc), including practical experience with **Finnish national registry data is a must for this role** • Strong **SAS or R** programming skills • Ability to u
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