Related skills
gcp clinical trials ich statistical programming cdisc📋 Description
- Lead or support programming efforts to deliver technical components of a project.
- Implement statistical programming aspects of the protocol and development program.
- Ensure high quality in own deliverables and those of other programmers.
- Program independently with high efficiency and quality.
- Write and/or implement specifications and oversee documentation completeness.
- Contribute to best practices to improve quality, efficiency, and effectiveness.
🎯 Requirements
- Bachelor's in CS/statistics or related field; 5+ years CDISC clinical programming.
- Master's in CS/statistics or related field; 6+ years CDISC clinical programming.
- Oncology Therapeutic Area experience.
- Knowledge of ICH and Good Clinical Practices (GCP).
- Understanding of the clinical drug development process.
- Strong communication and coordination skills.
🎁 Benefits
- Remote work opportunity.
- Contract position.
- Client-facing role on oncology projects.
- Global CRO with 28+ years of experience.
- Collaborative team with career development.
- Focus on quality and professional growth.
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