Associate Director, Statistical Programming
Bridgewater, New Jersey, United States; Remote, United States
R
USD 170K-205K Mid-level Full Time
Tasks
- Coach mentor develop statistical programming teams
- Conduct performance reviews and developmental planning
- Develop maintain clinical data statistical reporting standards
- Ensure quality timely within budget deliveries
- Lead client relationship management initiatives
- Manage clinical trial programs/projects
- Monitor data programming standards
- Participate in applicant interviews and evaluation process
- Perform QC review of statistical programming deliverables
- Provide technical operational leadership
- Provide technical review and advice
- Recommend implement improvements
- Review confirm ADaM dataset specifications
- Review confirm SDTM dataset specifications
- Review define documents and reviewer guides
- Review provide input to data management deliverables
- Review validate statistical tables listings figures
- Serve as principal level statistical programmer
Perks/Benefits
- 401k retirement plan
- Employee Assistance Program (EAP)
- Fitness reimbursement
- Paid time off
- Tuition reimbursement
Skills/Tech-stack
ADaM | Biostatistics | CDISC | Clinical trials | Data Management | Data Management Plan | Data Review Plan | Data Validation | Data programming | Data review | ECRFs | FDA | Quality Control | Regulatory Submissions | SDTM | Statistical programming | TLFs
Education
Regions
Countries
States
Cities
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