Lead and/or support programming for clinical projects.
Apply high technical skills to independently perform programming tasks.
Responsible for supporting programming deliveries of a study or project.
Implement statistical programming aspects of the protocol and development program.
Ensure high quality in own and others' deliverables.
Write/implement specs and oversee relevant documentation.

🎯 Requirements

Bachelor's degree in CS/statistics or related with 5 years CDISC experience.
Master's degree in CS/statistics or related with 6 years CDISC experience.
Oncology TA experience.
ICH/GCP knowledge and regulatory terminology.
Strong communication and coordination skills.

🎁 Benefits

Global CRO focused on quality and career development.
Supportive culture with strong client-facing collaboration.
28+ years; 4,000+ professionals in 20+ countries.
Equal opportunity employer promoting diversity and inclusivity.
Ongoing training keeps skills current.

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