DGM - Clinical Project Management Role

1. Plan study activities and timelines to share with stakeholders, set up tracking tools for assigned trials & assess progress as per pre-set timelines.

2. Prepare & obtain approval for clinical trial budget and for any change in the budget during the study.

3. Participate in vendor selection. Oversee & assess vendor performance, Vendor management.

4. Co-ordinate finalization of IP label & requisition. Forecasting of IP requirement during the study and prepare IP requisition.

5. Train study team on trial documents, processes & assigned SOPs.

6. Arrange/Participate in kick-off meetings.

7. Prepare/Review study plans & oversee compliance.

8. Plan and conduct IM if required.

9. Tracking of project finance & project milestones.

10. Meet investigators and key opinion leaders for assigned trials