Pr. Statistical Programmer (Clinical Pharmacology)
Tasks
- Conduct internal project meetings and track action items
- Create programming tools and macros
- Deliver concurrent programming timelines
- Develop SAS code for tables listings graphs derived datasets
- Develop dataset and output specifications
- Follow SOPs, WIs, and regulatory guidelines
- Maintain project documentation
- Manage scheduling across concurrent projects
- Mentor programming personnel
- Perform CDISC compliance reviews for SDTM and ADaM
- Perform validation programming
- Prepare DefineXML
- Provide CDISC guidance and training
- Provide risk mitigation plans
- Provide technical expertise for clinical programming questions
- Represent statistical programming in sponsor meetings
- Resolve programming discrepancies
- Review Statistical Analysis Plan mock shells and programming specifications
- Transfer deliverables
Perks/Benefits
- Career development
- Inclusive culture
- Peer recognition
- Supportive line management
- Technical and therapeutic training
- Total rewards program
Skills/Tech-stack
ADaM | Analysis Plan | CDISC | Clinical trial | Data Validation | DefineXML | ICH | Programming macros | Quality Control | S&OP | SAS | SDTM | Statistical Analysis | Statistical Analysis Plan
Education
N/A
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