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As a member of Parexel’s Statistical Programming group, you analyze, summarize, and graphically present clinical data to assess the safety and efficacy of the clinical trial. It requires attention to detail, a commitment to quality, and effective communication to ensure new treatments reach patients faster. You will work in different therapeutic areas assessing a variety of data entries and endpoints in an ever-changing environment. We provide a fertile environment for growth, with extensive training, mentoring, and technical knowledge sharing. You will work closely with the client and Parexel teams and collaborate to maximize the collective strength. Experience a supportive and motivating work environment where our teams offer an inherent breadth of knowledge within a diverse and inclusive workplace.
Job Responsibility:
Develop and validate SAS programs for datasets, tables, listings, and figures
Collaborate with global teams to support clinical trial analysis
Ensure compliance with CDISC standards and regulatory requirements
Support the electronic submission preparation and review
Reviews key planning documents (e.g., statistical analysis plan, data presentation plan, data review plan) to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements
Contribute to life-changing research in a flexible, remote-friendly environment
Requirements:
Proficiency in SAS (Base, Macro, and Graph)
Sound knowledge of CDISC standards (ADaM, SDTM)
Proven clinical / statistical programming experience within pharmaceutical clinical development (CRO/Pharma) - Minimum 3years experience is essential