CTC is a specialized search and recruitment partner for the Life Sciences industry, serving clients and candidates since 1997. We enable careers by connecting talented professionals with meaningful opportunities, and we support our clients in engaging, retaining, and developing the right talent when needed.
Headquartered in Switzerland – a biotech-hub of Europe – our client is a high-potential biopharmaceutical company, specialized in the discovery, development and commercialization of innovative small molecules, with the aim of transforming the horizon of therapeutic options in rare diseases.
Basel office, they’re currently looking for a:
Senior Statistical Programmer
This is an exciting opportunity to contribute to the development of innovative therapies through high-quality data analysis and reporting.
Main responsibilities:
* Implement and manage programs to analyze and report clinical trial data.
* Review trial documentation, provide programming input, and support study set-up in the reporting environment.
* Define project and trial analysis datasets and metadata.
* Design and implement complex data derivations, data mapping, and data pooling in collaboration with statisticians and trial programmers.
* Develop programs to generate Tables, Listings, and Figures (TLFs) for clinical reports and statistical analyses.
* Perform and document Quality Control (QC) in compliance with SOPs.
* Deliver trial outputs in line with project timelines and regulatory standards.
* Maintain documentation and archive trial data outputs in the eTMF.
* Support technical and system implementation to optimize data analysis workflows.
Qualifications and Experience:
* Relevant Swiss working/residency permit and/or Swiss/EU-Citizenship required.
* University degree (or equivalent) in Mathematics, Informatics, or a related scientific field.
* Minimum 5 years of experience in statistical programming, including experience in pharma or CRO settings.
* Advanced SAS programming skills and a strong understanding of statistical methods in clinical trials.
* Solid knowledge of CDISC standards, especially SDTM and ADaM.
* Basic knowledge of R and familiarity with other programming languages is a plus.
* Clear understanding of ICH-GCP and international clinical research regulations.
Would you like to learn more about CTC and the opportunity outlined? Please, get in contact with us: you may either use the 'apply now' button, or write an email to us, or reach out to us on the phone.
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