I am working for a MNC dealing with Clinical Data Management. Below are few points consideration.
Role of Clinical Data Management in Clinical research Industry
Your roles and responsibilities as Clinical data manager
Your knowledge about industry standards such as ICH-GCP, 21 CFR Part 11, GCDMP, CDISC etc.
Detailed understanding of all data management processes starting from CRF design (paper or electronic)
To final database lock.
For experienced data managers, real life examples are asked as – how you manage your trial time lines, resources, budget?
How do you ensure quality of data? How you handle conflict? Etc….
Hope above points are helpful to you.
All the best