Lead Statistical Programmer for Oncology Trials

ClinChoice; United Kingdom; On-site; GBP 70,000 - 90,000; Full time

Job summary

ClinChoice is seeking a Senior Statistical Programmer Consultant to join one of our client projects. This client-facing role delivers programming expertise under the Programming team lead, driving technical programming and deliverables with independence and high quality.

Requirements include a Bachelor's or Master’s in CS or statistics with CDISC experience and Oncology TA exposure, plus strong ICH/GCP knowledge and ability to coordinate with study teams.

Qualifications

• Degree in CS/statistics or related field with CDISC experience.
• Oncology TA experience is required.
• Knowledge of ICH/GCP and regulatory terminology is expected.

Responsibilities

• Support programming deliveries of a clinical study or project.
• Implement statistical programming aspects of the protocol and development program.
• Ensure high quality in own deliverables and in others' work.
• Program independently with high efficiency and accuracy.
• Create and oversee specifications and documentation.
• Contribute to best-practice improvements for quality and efficiency.
• Ensure compliance with standards and automation usage.
• Plan and support team activities and tasks.
• Communicate and escalate risks within studies/projects.
• Collaborate with statisticians, lead programmers, data managers and study leaders.

Skills

Statistical programming

CDISC

Oncology TA experience

Communication skills

Coordination skills

Independent work

Education

Bachelor's degree in CS/statistics or related

Master's degree in CS/statistics or related

Tools

CDISC (SDTM/ADaM)

ICH/GCP knowledge

Job description

ClinChoice is seeking a Senior Statistical Programmer Consultant to join one of our client projects. This client-facing role delivers programming expertise under the Programming team lead, driving technical programming and deliverables with independence and high quality.

Requirements include a Bachelor's or Master’s in CS or statistics with CDISC experience and Oncology TA exposure, plus strong ICH/GCP knowledge and ability to coordinate with study teams.