Senior Statistical Programmer, Regulatory Submissions
Merck & Co.
Merck & Co. is seeking a Senior Statistical Programmer in Rahway, NJ. This role oversees the quality of submission data standards for regulatory applications related to drug and vaccine clinical development. Candidates should have a BA/BS with 5 years of SAS programming experience or an MS with 3 years in a clinical trial environment. Key responsibilities include managing quality deliverables and guiding project teams while collaborating with stakeholders. Preferred candidates should also have skills in R, Python, and familiarity with CDISC standards. #J-18808-Ljbffr Merck & Co.
Vacancy posted 3 days ago
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