A biotech firm in Waltham, Massachusetts, is looking for an experienced Associate Director of Statistical Programming. This role involves leading statistical programming for clinical trials and regulatory submissions while managing relationships with CROs. Candidates should have a strong background in SAS programming and substantial experience in clinical development, particularly in late-phase trials. An advanced degree in a relevant field is required, along with a passion for advancing novel therapies for obesity and related conditions.
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Lead Statistical Programming & Submissions (CDISC) in waltham at Unknown Company
This position is listed as full time and onsite.