Job Summary
A clinical research organization needs applicants for an opening for a Telecommute Clinical Research Associate 3 .
Core Responsibilities Include:
- Identifying scientific misconduct at the site level
- Conducting monitoring to confirm subject safety and data ntegrity
- Applying knowledge of PRA's policies and procedures
Position Requirements Include:
- An advanced degree
- Knowledge of ICH and local regulatory authority regulations regarding drug
- 2+ years of clinical monitoring experience required
- Clinical research experience
- Knowledge of ICH and local regulatory authority regulations regarding drug
- Read, write and speak fluent English
