Description
Description:- Work under direction of COSTLs for assigned studies for activities including and not limited to, ensuring study monitoring and data management tasks undertaken by CROs progress to agreed timelines; inspection readiness preparation.
Critical Skills:
- Team work
- Interpreting metrics
- Knowledge of monitoring and data management for clinical trials
- Understanding components of a trial master file
- CRO staff management.
- Ability to take direction from peers
- Ability to work independently,
- Attention to detail
- MS Word