Related skills
gcp clinical trials cdisc oncology clinical data programming📋 Description
- Lead and/or support programming work for a clinical study or project.
- Implement statistical programming aspects of the protocol.
- Ensure high quality in own deliverables and others' work.
- Program independently with high efficiency and quality.
- Write/implement specifications; oversee documentation.
- Plan and support study team activities; manage risks.
🎯 Requirements
- Bachelor’s in CS, statistics, or related field; 5 yrs CDISC clinical programming.
- Master’s in CS/statistics with 6 yrs CDISC experience.
- Oncology TA experience.
- Knowledge of ICH-GCP, clinical research, and trial processes.
- Strong communication and coordination skills.
- Ability to influence stakeholders on programming items.
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