Centralized Clinical Trial Manager

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

• 8–10 years in pharma & medical sales
• Clinical research
• SOP writing
• Communication
• Any graduate

Good to have

• Two-wheeler

What you get