Related skills
documentation gcp clinical trials ich statistical programming📋 Description
- Lead and/or support programming deliveries for a clinical study.
- Implement statistical programming tasks for protocol and development program.
- Ensure high quality in own deliverables and in others' work.
- Program independently with efficiency and quality.
- Write and review specifications; ensure complete documentation.
- Plan and support study team activities; escalate risks.
🎯 Requirements
- Bachelor's in CS or statistics; 5 yrs clinical programming (CDISC).
- Master's in CS/statistics; 6 yrs CDISC programming.
- Oncology TA experience.
- Working knowledge of ICH and GCP regulatory requirements.
- Understanding of the clinical drug development process.
- Strong communication and coordination skills.
🎁 Benefits
- Global full-service CRO with quality focus.
- Professional development opportunities.
- Supportive, high-trust client environment.
- Equal opportunity employer.
- Long-term career opportunities.
- Collaborative, team-oriented culture.
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