
Data Standards Programmer
2 weeks ago
About This Role
We are seeking a skilled professional to join our clinical team. The successful candidate will have experience in programming support for clinical trials and be responsible for implementing data standards, following regulatory requirements.
Key Responsibilities
- Provide programming support for clinical trials, ensuring high-quality statistical outputs.
- Implement CDISC and other industry data standards, following internal programming conventions.
- Serve as lead on assigned studies, coordinating activities with support programmers.
- Create project timelines and develop tools to improve quality and efficiency of processes.
- Prepare programming specifications for SDTM, ADaM, and other derived datasets, applying knowledge of SAS programming.
- Perform ad hoc analyses of current and legacy databases, reviewing case report form design.
- Serve as mentor to other programmers, maintaining awareness of scope of work and alerting management to potential change orders or resourcing needs.
Requirements
- Bachelor's degree in Statistics, Computer Science, or closely related field; or equivalent experience.
- Minimum 4 years direct SAS programming experience in pharmaceutical development or CRO environment.
- Knowledge of medical terminology, conduct, and analysis of clinical trials.
- Knowledge of relevant industry data standards (e.g. CDISC SDTM, ADaM).
What We Offer
- A diverse and inclusive work environment, committed to diversity and inclusion.
- A challenging role that offers opportunities for growth and professional development.
- A collaborative team environment that values innovation, creativity, and teamwork.
About Our Organization
We are a clinical development and strategic resourcing organization committed to improving the lives of those touched by clinical research. Our goal is to provide a better clinical experience across the drug development journey, approaching each opportunity with foresight, character, resilience, and innovation.
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