1002# Sr Principal/ Principal Statistical Programmer Consultant- Oncology (Remote)
Skills
- Strong SAS programming and clinical programming experience in CDISC standards.
- Expertise in Oncology/Hematology therapeutic area.
- Experience with ISS and ISE reports.
- Understanding of ICH guidelines, Good Clinical Practices, and clinical drug development process.
- Excellent communication and coordination skills.
- Ability to manage concurrent project activities proactively.
Responsibilities
- Develop Tables, Figures, Listings (TFLs) deliverables from existing or new SAS programs for Clinical Study Reports.
- Independently program and review clinical study reports and outputs with high efficiency and quality.
- Customize outputs and graphics per biostatisticians' specifications.
- Support programming delivery for clinical studies or projects ensuring compliance with standards.
- Contribute to best practice development to improve quality and efficiency.
- Plan and support team activities and communicate project risks proactively.
Education
- Bachelor’s degree in Computer Science, Statistics, or related scientific discipline with 10 years clinical programming experience or
- Master’s degree in related field with 8 years clinical programming experience.
Benefits
- Opportunity to work with a global CRO with over 28 years of experience.
- Professional development and continuous training.
- Inclusive and diverse workplace culture.
- Remote work flexibility.
Average salary estimate
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