Centralized Clinical Trial Manager
Bengaluru, ChennaiFull-time8–10 yrsPosted 4 days ago
Senior pharma role at ICON India Clinical - in Bengaluru and Chennai. Needs 8–10 years.
About the role
As a Centralized Clinical Trial Manager at ICON, you will play a crucial role in effectively reviewing site visit reports as per Protocol and ICON and Sponsor SOPs and to ensure the quality of reports are of the highest standards , errors are minimized and that issues are escalated as appropriate. You will be responsible for follow up on action items and protocol deviations and to be a liaison between CRA, CTM and PM for timely resolution of issues.
What you'll do
- Follow up on action items and protocol deviations and to be a liaison between CRA, CTM and PM for timely resolution of issues
- Act as an extension of the CTM/CTM team for the specific purpose of visit report review and approval
- Observe and escalate safety trends in patients as identified in visit report
- As a Manager, the employee is expected to recognize the importance of and create a culture of process improvement with a focus on streamlining our processes adding value…
- Regular oversight of OMR , ICO trial (and where required Sponsor CTMS and vendor systems) to ensure key metrics, e.g. MVR and FUL timelines
What you need
- Clinical research
- Learning and development
- SOP writing
- Communication