Senior Statistical Programmer/Analyst Consultant -Early Phase Oncology -Remote in UK
Related skills
gcp clinical trials ich statistical programming cdisc📋 Description
- Leads and supports programming deliverables for a clinical study.
- Implements statistical programming aspects of the protocol.
- Ensures high quality in own deliverables and others' work.
- Programs independently with high efficiency and quality.
- Writes/implements specifications; oversees documentation.
- Plans and supports study team activities; communicates risks.
🎯 Requirements
- Bachelor's degree in CS/statistics or related field with 5 yrs CDISC clinical programming.
- Master's degree in CS/statistics with 6 yrs CDISC clinical programming.
- Oncology TA experience required.
- Working knowledge of ICH, GCP, clinical trial regulatory terms.
- Strong communication and coordination skills.
- Proficient understanding of clinical drug development process.
🎁 Benefits
- Global CRO with professional development opportunities.
- Equal opportunity employer.
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