Related skills
data management gcp sas clinical trials statistical programming📋 Description
- Lead and/or support programming efforts on a clinical study.
- Deliver technical programming for the clinical development program.
- Ensure high quality in own deliverables and others' outputs.
- Plan and execute programming tasks with efficiency and quality.
- Collaborate with study team (Statistician, Lead Programmer, Data Manager).
🎯 Requirements
- Bachelor’s degree in CS/statistics; 5 yrs CDISC clinical programming.
- Master’s degree in CS/statistics; 6 yrs CDISC clinical programming.
- Oncology TA experience.
- Knowledge of ICH/GCP and regulatory requirements.
- Strong communication and coordination skills.
- Proven ability to influence programming-related decisions.
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