Job description
Essential Functions:
- Writing Statistical Analysis Plans
- Consulting with clients on study design, including sample size calculations
- Writing internal SAS programming instructions
- Reviewing statistical documents
- Writing statistical sections for a clinical study protocol
- Reviewing tables, listings, and figures
- Writing statistical analysis reports and the statistical sections for a clinical study report
- Interacting with regulatory authorities
Additional Responsibilities:
- Leading periodic team meetings (meeting agendas and minutes) either internal or with the sponsors.
- Provide monthly progress reports.
- Review/Update internal documents related to the conduct of clinical trials.
Job Qualifications: General Knowledge, Skills, and Abilities (KSA’s) required
- A PhD in Statistics or Biostatistics
- Understanding of clinical trials
- Excellent oral and written communication skills
- Ability to work both independently and in a team environment
- Proficiency with Microsoft Word
- Excellent SAS® programming skills
- Ability to multi-task and think on your feet
Job Type: Contract
Salary: $90,000.00 - $100,000.00 per year
Schedule:
- 8 hour shift
Ability to commute/relocate:
- North Fairfield, OH 44855: Reliably commute or planning to relocate before starting work (Required)
Work Location: One location
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