Contractor - Senior statistical programmer - Remote

Key Responsibilities: Preference for candidates in EST or a similar time zone 5–10 years of clinical trial programming experience Strong Phase 2/Phase 3 experience, with an emphasis on ADaM dataset programming and TFL development Strong SDTM experience is preferred but not required Ability to work independently, including programming without detailed data specifications Experience supporting internal data requests and working in a fast-paced, growing environment Ability to prioritize urgent requests and multitask effectively Asthma experience is a plus but not required Submission experience is also a plus Experience with R and/or Python is a nice-to-have Preference for candidates who have worked within a small-to-midsize sponsor environment

Qualifications: Bachelor’s or Master’s degree in Statistics, Computer Science, or a related field. Minimum 5 years of relevant experience in the biopharmaceutical, biotechnology, or CRO industry. Experience in late-phase (phase III) trials is highly desirable. Proficiency in SAS programming. Hands-on experience with raw datasets, SDTM, and ADaM dataset development. Strong analytical, problem-solving, and communication skills (both verbal and written).Ability to work effectively in a cross-functional environment, proactively influencing teams with innovative clinical development strategies.