Opportunity Description
**Work Schedule**
Second Shift (Afternoons)
**Environmental Conditions**
Office
**Job Description**
Join Us as a **Clinical Review Specialist** – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our global team, you’ll have the opportunity to review patient data with a high level of accuracy. As a Clinical Review Specialist, you'll ensure that all tasks are conducted in accordance with Good Clinical Practice (GCP), Standard Operating Procedures (SOPs)/Working Practice Documents (WPDs), and Data Validation Manuals (DVMs). You will liaise with colleagues in other functional groups as required and communicate with management for all data review activities within your allocated studies.
What You’ll Do:
• Reads and understands project protocols an...
Second Shift (Afternoons)
**Environmental Conditions**
Office
**Job Description**
Join Us as a **Clinical Review Specialist** – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.
As part of our global team, you’ll have the opportunity to review patient data with a high level of accuracy. As a Clinical Review Specialist, you'll ensure that all tasks are conducted in accordance with Good Clinical Practice (GCP), Standard Operating Procedures (SOPs)/Working Practice Documents (WPDs), and Data Validation Manuals (DVMs). You will liaise with colleagues in other functional groups as required and communicate with management for all data review activities within your allocated studies.
What You’ll Do:
• Reads and understands project protocols an...
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