1. Clinical Research and History

2. Clinical Drug Development

3. ICH-GCP guideline/ IEC IRB responsibilities

4. 21 CFR part 11/ Clinical trials

5. Clinical data management basic information

6. Clinical databases and types

7. Set up phase- Protocol/ CRF design/ Edit Check Specification document

8. Data Management Plan/User Acceptance Testing/ SAE document/CRF completion guideline.

9. Conduct phase- Data entry/ Medical coding/ Data cleaning

10. SAE recon/External data reconciliation/ Discrepancy management

11. Study closeout

12. Archival

Skill development classes

1) Resume preparation

2) How to search jobs

3) Expert advice

4)HR interview question discussion

5)Mock interview

course Benefits

1) Certificate from ISO certified organization which is accepted worldwide

2) 100% placement assistance

3) Recorded lectures provided after live

4) Learn from top industry experts working professionals from top MNC in india