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Note: The job is a remote job and is open to candidates in USA. Parexel is a global leader in clinical development solutions, dedicated to improving the world's health. They are seeking a Statistical Programmer II to develop and validate SAS programs, collaborate with global teams for clinical trial analysis, and ensure compliance with regulatory standards.
Responsibilities
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
Skills
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 3 years experience is essential
Strong analytical and communication skills
Benefits
Career growth and mentorship
Fully remote work options
A culture of integrity, respect, and innovation
Company Overview
Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. It was founded in 1983, and is headquartered in Raleigh, North Carolina, US, with a workforce of 10001+ employees. Its website is http://www.parexel.com.
Company H1B Sponsorship
Parexel has a track record of offering H1B sponsorships, with 33 in 2025, 46 in 2024, 41 in 2023, 51 in 2022, 54 in 2021, 33 in 2020. Please note that this does not guarantee sponsorship for this specific role.
