About the Role
Trialt is expanding its Statistical Programming team to support international Phase
What You Will Do
• Lead statistical programming activities across one or more clinical studies.
• Oversee the development and validation of SDTM, ADaM and TLF deliverables.
• Plan programming work, estimate timelines and coordinate task allocation.
• Review complex deliverables and ensure compliance with project, CDISC and regulatory requirements.
• Maintain traceability from source data through SDTM and ADaM to final statistical outputs.
• Support the preparation and review of Define-XML, aCRF, SDRG, ADRG and validation reports.
• Investigate and resolve complex programming, data and submission-readiness issues.
• Lead client-facing meetings and technical discussions.
• Monitor project quality, timelines, risks and programming status.
• Mentor programmers and provide technical leadership.
• Collaborate closely with biostatistics, data management, medical writing and project management teams.
Required Qualifications
• Extensive statistical programming experience within clinical research.
• Advanced SAS programming skills and strong knowledge of CDISC SDTM and ADaM standards.
• Extensive experience producing and independently reviewing SDTM, ADaM and TLF deliverables.
• Experience leading programming activities at study or project level.
• Strong understanding of regulatory submission requirements and end-to-end traceability.
• Experience reviewing submission documentation and resolving Pinnacle 21 findings.
• Ability to plan work, estimate timelines, oversee quality and manage programming risks.
• Strong client-facing communication and technical leadership skills.
• Ability to mentor programmers and make independent technical decisions.
• English at Upper-Intermediate level or higher.