Senior Statistical Programmer/Analyst Consultant – Hybrid

ClinChoice

. Support programming deliveries for a clinical study or project .

Posted 10/23/2026contractUnited StatesSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical programming, particularly in CDISC standards, while ensuring compliance with ICH and Good Clinical Practices. Proficient in managing project activities and communicating effectively with stakeholders to enhance programming quality and efficiency.

Highest-signal resume keywords

Clinical Programming (CDISC)Bachelor's Degree in Computer Science or StatisticsICH and Good Clinical Practices KnowledgeStrong Communication SkillsProject Management

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical ProgrammingProtocol ImplementationDocumentation OversightQuality AssuranceAutomation Usage

Soft Skills

Coordination SkillsProactive Risk ManagementStakeholder Influence

Industry Keywords

Clinical ResearchClinical Trial ProcessesRegulatory RequirementsClinical Drug Development

About the role

Key responsibilities & impact

Support programming deliveries for a clinical study or project
Implement statistical programming aspects of protocols and clinical development programs
Ensure high quality in personal and other programmers’ deliverables
Program independently with high efficiency and quality
Write or implement specifications and oversee relevant documentation completeness
Contribute to best practices improving quality, efficiency, and effectiveness
Ensure compliance with standards and automation usage
Plan and support team activities and tasks
Communicate and escalate risks within assigned studies or projects
Work proactively with Statisticians, Lead Programmers, Data Managers, and Study Leaders

Requirements

What you’ll need

Bachelor’s degree in computer science (CS), statistics, or related scientific disciplines with 5 years of clinical programming (CDISC) experience; or Master’s degree in CS, statistics, or related disciplines with 6 years of clinical programming (CDISC) experience
Working knowledge of ICH and Good Clinical Practices, clinical research, clinical trial processes, and related regulatory requirements and terminology
Good understanding of the clinical drug development process
Strong communication and coordination skills
Current knowledge of technical and regulatory requirements relevant to the role
Ability to proactively manage concurrent activities within a project
Proficient ability to influence relevant stakeholders on programming-related items

Benefits

Comp & perks

Professional development and supportive culture
Close management and training
Continuous training and development opportunities
Equal opportunity, diversity, and inclusivity
Opportunity to work directly for a single sponsor with the security and career opportunities of a global CRO