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Senior Statistical Expert
2 weeks ago
Job Summary
As a seasoned statistical programmer, you will play a vital role in delivering high-quality statistical outputs to support drug development across the clinical research journey.
Our team is dedicated to exceeding expectations and pushing the boundaries of innovation. We are seeking a skilled and experienced statistical programmer to join our dynamic team.
Key Responsibilities
- Develop and implement CDISC and other regulatory standards to ensure compliance and quality.
- Collaborate with cross-functional teams to design and develop innovative solutions that improve efficiency and quality.
- Provide programming specifications for SDTM, ADaM, and other derived datasets to support data analysis and reporting.
- Develop and maintain project timelines to ensure timely delivery and high-quality results.
- Apply knowledge of SAS programming to develop and validate statistical outputs according to the statistical analysis plan and other specifications.
Requirements
- Minimum 4 years direct SAS programming experience in pharmaceutical development or CRO environment.
- Good knowledge of medical terminology and conduct and analysis of clinical trials.
- Excellent oral and written communication skills, organizational skills, and attention to detail are required.
Diversity and Inclusion
We believe that diversity and inclusion are crucial to fulfilling our mission and demonstrating our values. A diverse staff allows us to effectively draw on different perspectives and enhance our efficiency and effectiveness.