Elevate your career as a Senior Statistical Analyst, specializing in SAS programming and analysis dataset development. Join a agile team focused on pharmaceutical data solutions.This role requires solid skills in developing and validating analysis datasets (ADaM) and TFLs using SAS. You will lead programming projects, manage timelines, and mentor junior programmers while maintaining compliance with ICH-GCP and CDISC standards. Your expertise in clinical trials and statistical methods will be key in communicating with clients and delivering high-quality outputs.Key Responsibilities:
Develop and validate analysis datasets and TFLs in SAS
Write and review programming specifications and documentation
Create macros and tools to enhance efficiency




Lead programming projects and mentor team members
Oversee SAS code reviews and quality standards complianceRequirements:
Bachelor’s degree in Statistics or related field
3+ years of SAS programming experience in CRO settings
Strong knowledge of clinical trials and regulatory requirements
Proven experience in leading programming projects
Excellent communication skills with global teamsUtilize your SAS expertise to deliver impactful results and support team growth in the pharmaceutical sector.#J-18808-Ljbffr

📌 Senior Statistical Analyst With Sas Expertise Newmarket
🏢 Bilinguallink
📍 Newmarket