Statistical Programming Associate Director
Tasks
- Apply project management practices for drug or technical projects
- Develop best practices for quality efficiency and effectiveness
- Drive standards development and implementation
- Ensure compliance to standards and automation usage
- Ensure high-quality project deliverables
- Identify methodology improvement opportunities and provide solutions
- Lead implementation of statistical programming aspects of protocols
- Lead or contribute to process improvement initiatives
- Manage and escalate project and study risks
- Manage external partner activities
- Provide input to capacity management
- Provide programming expertise to the team
- Provide programming subject matter expertise to stakeholders
- Provide tactical inputs and improvement ideas
- Support recruiting, training, and mentorship
Perks/Benefits
- N/A
Skills/Tech-stack
CDISC | Clinical Development | Clinical development process | Clinical trial | Clinical trial management | Development Process | Programming | R | SAS | SAS Macros | Trial management
Education
Bachelor of Engineering | Bachelor of Science | Master of Science | PhD
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