Associate Director, Statistical Programming
Bridgewater, New Jersey, United States; Remote, United States
R
USD 170K-205K Mid-level Full Time
Tasks
- Coach and mentor statistical programming teams
- Create training curricula and governing documents
- Develop clinical data and statistical reporting standards
- Lead client relationship and business development initiatives
- Lead performance review and development plans
- Manage clinical trial programs
- Oversee client program quality on time budget
- Perform QC review of statistical programming deliverables
- Provide input to eCRFs and data validation specifications
- Provide technical leadership to project teams
- Review and improve programming standards
- Review define documents and reviewer guides
- Review statistical tables listings figures
- Support clinical data management deliverables
- Validate ADaM datasets
- Validate SDTM datasets
Perks/Benefits
- 401k retirement plan
- Disability insurance
- Employee assistance program
- Fitness reimbursement
- Life insurance
- Medical, dental & vision coverage
- Paid time off
- Performance bonus
- Remote work option
- Tuition reimbursement
Skills/Tech-stack
ADaM | Agency support | Biometrics | Biostatistics | CDISC | Clinical trial | Clinical trial management | Communication skills | Data Management | Data Management Plan | Data Review Plan | Data Validation | Data review | Define.xml | ECRF | Electronic Regulatory Submissions | FDA Submissions | Project Planning | Quality Control | Regulatory Submissions | Regulatory agency support | SDTM | Statistical programming | TLF | Team leadership | Trial management
Education
Roles
Associate | Associate Director | Director | Programmer | Statistical Programmer
Regions
Countries
States
Cities
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