Related skills
documentation programming gcp clinical trials ich📋 Description
- Supports programming deliveries for a clinical study or project.
- Implements statistical programming aspects of the protocol.
- Ensures quality in own deliverables and by other programmers.
- Programs independently with high efficiency and quality.
- Writes specifications and oversees relevant documentation.
🎯 Requirements
- Bachelor's degree in CS, statistics, or related field with 5 years CDISC clinical programming.
- Master's degree in CS, statistics, or related with 6 years CDISC clinical programming.
- Oncology TA experience.
- ICH, GCP, and clinical trial regulatory knowledge.
- Strong understanding of the clinical drug development process.
- Strong communication and coordination skills.
🎁 Benefits
- Direct sponsor exposure with CRO career growth.
- Global CRO with training and professional development.
- Equal opportunity employer with diverse, inclusive culture.
- Structured training and ongoing professional development.
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