Senior Statistical Programmer / Analyst Consultant – Oncology (Remote – US, Contract)
Location: United States (Remote)
Employment Type: Contract / Full-Time
Experience Required: 5–6+ Years in Clinical Programming (CDISC)
Educational Qualification: Bachelor’s or Master’s in Computer Science, Statistics, or related scientific discipline
Job Overview
ClinChoice, a global full-service CRO, is seeking a Senior Statistical Programmer / Analyst Consultant with Oncology therapeutic area (TA) expertise. This role combines advanced programming skills, CDISC knowledge, and regulatory awareness to deliver high-quality clinical programming outputs.
The ideal candidate will work independently under Programming team leadership, supporting end-to-end statistical programming for oncology clinical trials while ensuring regulatory compliance, data integrity, and efficient project delivery.
Key Responsibilities
Statistical Programming & Deliverables
Lead or support programming activities for assigned oncology studies.
Develop and implement statistical programming components of study protocols and clinical development programs.
Ensure high-quality, compliant, and traceable outputs for all programming deliverables.
Write, implement, and review programming specifications; oversee completeness of documentation.
Program independently with efficiency while mentoring or supporting junior team members.
Process Improvement & Compliance
Contribute to best practices for programming efficiency, quality, and effectiveness.
Ensure compliance with internal standards, automation protocols, and regulatory requirements (ICH, GCP).
Plan and support team activities and task allocation.
Identify, communicate, and escalate risks within assigned studies or projects.
Collaboration & Coordination
Work closely with Statisticians, Lead Programmers, Data Managers, and Study Leaders.
Support integrated analyses and cross-functional project needs.
Influence stakeholders on programming-related items and deliverables.
Required Qualifications
Bachelor’s degree in Computer Science, Statistics, or related discipline with 5 years of clinical programming experience, or Master’s degree with 6 years of experience.
Hands-on experience with CDISC SDTM and ADaM datasets.
Oncology therapeutic area experience (hematologic or solid tumors).
Understanding of clinical drug development processes, ICH guidelines, and Good Clinical Practices (GCP).
Strong knowledge of clinical trial terminology and regulatory requirements.
Excellent communication, coordination, and stakeholder management skills.
Ability to manage concurrent programming activities independently.
Why Join ClinChoice?
Work directly for a single sponsor while leveraging the resources and career opportunities of a global CRO.
Support Oncology clinical trials with high-impact programming responsibilities.
Join a culture of professional development, training, and high-quality delivery.
Contribute to innovation, automation, and best practices in clinical programming.
Work in a diverse and inclusive environment with global exposure.
Apply now to join ClinChoice as a Senior Statistical Programmer / Analyst Consultant – Oncology and play a critical role in regulatory-compliant clinical trial programming for oncology studies.
Discover more clinical programming and oncology roles on thepharmadaily.com.
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