Statistical Programmer H/F - 75

Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions guided by our values Energy, Care and Audacity.

Founded in 2014 and headquartered in Paris, France, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas.

We take a one-team approach to work : our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.

Excelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.About the Job

Join Excelya, whereAudacity, Care, and Energydefine who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth GO hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Safety. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Activities :
- Develop and maintain SAS programs for the reporting and analysis of clinical trial data.
- Collaborate with statisticians and clinical data managers to ensure statistical integrity of the results.
- Conduct exploratory statistical analyses and prepare summary statistics and tables as required.
- Create and validate datasets, ensuring accuracy and consistency across all outputs.
- Support ad-hoc requests for data analysis and create programming specifications.
- Participate in the development of programming practices and standards to improve efficiency and accuracy.
- Document work processes and ensure compliance with regulatory standards.
- Assist in the preparation of regulatory submissions as needed.