Director, Statistical Programming
Tasks
- Collaborate with cross functional teams for analysis reporting timelines
- Develop and maintain data review reporting tools
- Ensure timely high quality analysis reporting for regulatory approval
- Implement company data standards and submission standards
- Lead programming deliverables through regulatory submission
- Manage standards and project implementation to meet milestones
- Manage statistical programming activities across clinical studies
- Provide leadership for programming priorities and communication
- Provide technical input to statistical documents
- Represent programming in multidisciplinary clinical trial teams
Perks/Benefits
- Employee stock purchase plans
- Employee wellbeing benefits
- Fitness reimbursement
- Generous vacation time
- Long-term incentives
- Professional development plans
- Public holidays
- Remote work
- Tuition sponsorship
- Volunteer days
Skills/Tech-stack
ADaM | CDISC | Clinical Trial Programming | Clinical trial | Controlled Terminology | Data Analysis | Data Standards | Data review | Data review tools | Define-XML | ECTD | R | Review tools | Reviewer-Guide | S-Plus | SAS | SDTM | Statistical Data Analysis | Statistical data | Statistical programming | Vendor management
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