Job Description:
- $22 - $24/hour based on experience and education.
- 5 days on-site in North Chicago, hours are flexible (start between 5:00AM – 9:30AM, 8 hour day)
- This group supports many different groups who generate reports.
- Reports are received and quality checks are performed before they are submitted to the FDA.
- Day to day is involved with heavy documentation and MS Word in a GLP environment.
- High School Diploma required, Bachelor’s degree preferred.
- Detail-oriented, strong communication, not afraid to ask questions, work in a fast-paced environment, strong ability to prioritize tasks.
- Regulatory submissions experience is preferred, but not required.
- Previous office work – administrative assistant, strong MS Office skills.