Study Director
On-site · Durham, North Carolina, United States
Job Summary
Oversee and coordinate client studies, supervise and coordinate activities, and lead the execution of assigned studies. Provide strategic and technical oversight on studies, identify process improvements, draft study plans and contribute to sponsor reports. Ensure GLP compliance, approve and follow study protocols, accurately record and verify all data, and document any corrective actions. Ensure adherence to study protocols, complete archiving of raw data and final reports, and contribute to SOPs and forms. Maintain Good Documentation Practices, review literature to support studies, and supervise or train team members as needed. Travel up to 5% may be required. Proficiency in technical writing and data analysis is required; JMP familiarity and MS Office skills (Word, Excel, PowerPoint, Teams) are a plus.
Required Qualifications
- Bachelor’s degree in relevant scientific field (e.g. Chemistry, Biology, etc.)
- 3-5 years of relevant experience
- Proficiency in technical writing
- Must be able to analyze data sets and interpret results
- Familiarity with JMP is a plus, but not required
- Proficiency with Microsoft Office (Word, Excel, PowerPoint, Teams, etc.) required.
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