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Résumé du poste
A leading pharmaceutical firm is seeking a Principal Statistical Programmer to play a crucial role in the delivery of innovative projects. You will oversee programming activities and collaborate with various departments while mentoring less-experienced team members. The ideal candidate has over 5 years' experience in statistical programming within clinical trials and possesses expert knowledge of SAS and clinical trial processes. This position offers flexibility with the option to work fully remote in EMEA or from a local office. Fluency in English is a must.
Qualifications
5+ years of experience in statistical programming within clinical trials.
Expert knowledge of base SAS and SAS macros.
Broad knowledge of CDISC requirements related to SDTM and ADaM.
Fluency in English, both verbal and written.
Responsabilités
Plan and oversee programming activities on studies.
Oversee SDTM, ADaM and TLF development.
Liaise with other departments for programming needs.
Support submission activities, especially in late phase.
Mentor less-experienced team members in best practices.
Connaissances
Statistical programming
SAS programming
Clinical trials knowledge
Collaboration
Attention to detail
Mentorship
Formation
Degree in mathematics, life sciences, statistics, or computer sciences
Outils
SAS
CDISC standards
Description du poste
A leading pharmaceutical firm is seeking a Principal Statistical Programmer to play a crucial role in the delivery of innovative projects. You will oversee programming activities and collaborate with various departments while mentoring less-experienced team members. The ideal candidate has over 5 years' experience in statistical programming within clinical trials and possesses expert knowledge of SAS and clinical trial processes. This position offers flexibility with the option to work fully remote in EMEA or from a local office. Fluency in English is a must.
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