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Responsibilities:
- Lead statistical programming efforts for clinical studies.
- Oversee and coordinate activities with Contract Research Organizations (CROs).
- Conduct independent validation and quality checks of statistical programming deliverables from CROs.
Required Qualifications:
- Proven hands-on experience in programming for clinical development.
- Expertise in SAS programming and comprehensive knowledge of CDISC standards.
- Extensive experience overseeing CROs, including independent validation of datasets and statistical deliverables.
Preferred Qualifications:
- Background in cardiometabolic diseases or related therapeutic areas is preferred.
Kailera
Kailera is developing therapies that give people the power to transform their lives and elevate their overall health. Rooted in an entrepreneurial spirit and a team-oriented culture, they are working together to advance novel therapies for obesity and related conditions.