Role at a glance
- Job function
-
Healthcare Other
- Salary
- Not Disclosed
- Location
- Austin, Texas, United States
- Work arrangement
- On-site
- Employment
- Full-time
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Role Summary
The Project Assistant manages essential regulatory documents for studies and facilitates IRB submissions and other regulatory tasks, including study-training compliance. The role also ensures study files remain audit ready.
What You'll Do
- Manage essential regulatory documents for each study.
- Facilitate IRB submissions.
- Handle other regulatory tasks, such as study-training compliance.
- Ensure files are audit ready.
Generated from the employer's posting. Verify important details before applying.
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Original job description
Content provided by the employer
Original job description
Content provided by the employer
Work Schedule
Standard Office Hours (40/wk)Environmental Conditions
OfficeJob Description
The Project Assistant role is critical for managing each study's essential regulatory documents, facilitating IRB submissions and other regulatory tasks (like study training compliance), as well as ensuring files are audit ready at all times.
About the company
Thermo Fisher Scientific
Large Enterprise
Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.