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 understand written documentation of Finnish register data
•    CRO and/or pharmaceutical industry experience
•    Strong communication skills in English
•    Ability to manage multiple tasks and deliver high quality outputs within agreed timelines

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 at https://jobs.iqvia.com

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.