Manager, Statistical Programming (Oncology) > SEC Life Sciences > Joboolo BE :
Société : SEC Life Sciences Lieu : Site source : Talent BE
Your Role:
Lead programmatic reviews of datasets and statistical outputs to ensure top-notch quality for pivotal studies and regulatory submissions.Oversee project timelines and execution with statisticalprogramming vendors to guarantee quality deliverables on schedule.Drive the development of programming standards to enhance efficiency and quality in oncology research.Offer essential programming support for regulatory submissions, including swift responses to regulatory agencies.Craft and maintain programming macros for thorough internal data review and monitoring.Experience and Qualifications:
Strong experience in the pharmaceutical or CRO industry, specifically in clinical trials programming.Proven lead experience at the study-level, with a preference for candidates with prior exposure in Oncology Therapeutic Areas (TA).Advanced proficiency in SAS, CDISC SDTM, and ADaM standards, with a robust understanding of statistical concepts.Demonstrated ability to support global development projects through to regulatory submissions.Exceptional project management, organisational, and problem-solving skills.Flexibility to commit to US working hours, including availability for occasional meetings during US hours.This role is suited for a dynamic professional eager to make an impact in the field of statisticalprogramming and oncology.
If you're ready to contribute to meaningful advancements in cancer treatment and meet the above criteria, we encourage you to apply now for immediate consideration.
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