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ClinChoice
Data Science & Analytics 1h ago

Senior Statistical Programmer Consultant

ClinChoice
United StatesUnited States
Contract
Not Disclosed
Senior-Level

Job Description

Key Skills Required

Master these to land this role

CDISCStatistical ProgrammingClinical ResearchRegulatory ComplianceData Scientist

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ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of their clients. This role is client-facing and requires confident candidates who can work independently while establishing a high-trust environment with the client’s counterparts.

Main Job Tasks and Responsibilities:

The Senior Statistical Programmer Consultant is a delivery-focused role responsible for leading and/or supporting technical programming and information components of a project. This position requires high technical skills and thorough industry knowledge to independently perform programming tasks.

Key Responsibilities:

  • Supporting the programming deliveries of a clinical study or project.
  • Implementing statistical programming aspects of the protocol and the clinical development program.
  • Ensuring high quality in deliverables and those delivered by other programmers.
  • Programming independently with high efficiency and quality.
  • Writing and/or implementing specifications and overseeing completeness of relevant documentation.
  • Contributing to the development of best practices to improve quality, efficiency, and effectiveness within the function.
  • Ensuring compliance with standards and automation usage.
  • Planning and supporting team activities and tasks.
  • Communicating and escalating risks within the assigned studies and/or projects.
  • Working proactively with study team members, including but not limited to the Statistician, Lead Programmer, Data Manager, and Study Leader.

Education and Experience:

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

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ClinChoice is a leading global Clinical Research Organization (CRO) dedicated to accelerating the development and commercialization of innovative drugs, medical devices, and diagnostics. Founded in 1995 and headquartered in Horsham, Pennsylvania, the company operates with a massive global footprint, boasting over 3,000 clinical experts across the Americas, Europe, and Asia. Under the hood, ClinChoice delivers end-to-end full-service and Functional Service Provider (FSP) solutions—spanning clinical operations, biometrics, regulatory affairs, and post-marketing safety. Their primary target audience includes emerging and mid-sized biotech startups, as well as top-tier global pharmaceutical giants (partnering with 6 of the top 10 pharma companies globally). What sets ClinChoice apart in the highly regulated life sciences sector is its deep therapeutic expertise and tech-enabled delivery model, having successfully supported over 3,000 clinical studies and 10,000 regulatory submissions worldwide to bring life-saving treatments to market faster.

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