roles as part of our growing Functional Service Provider (FSP) team.
What you'll do:
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
What you'll bring:
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
Strong analytical and communication skills
What we offer:
Career growth and mentorship
Fully remote work options
A culture of integrity, respect, and innovation
Whether you're advancing your career or bringing senior-level expertise, Parexel empowers you to make a meaningful impact.
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