Lead and/or support programming deliverables for a clinical study.
Implement statistical programming aspects of the protocol and development program.
Ensure high quality in own deliverables and in others' outputs.
Program independently with high efficiency and quality.
Write and/or implement specifications and oversee relevant documentation.
Plan and support study team activities; communicate risks to the project.

🎯 Requirements

Bachelor’s or Master’s in CS/statistics or related with 5–6 yrs CDISC clinical programming.
Oncology TA experience.
Working knowledge of ICH and GCP, regulatory requirements and terminology.
Understanding of the clinical drug development process.
Strong communication and coordination skills; ability to influence stakeholders on programming items.
Ability to proactively manage concurrent activities and plan tasks while collaborating with the study team.

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