Centralized Clinical Trial Manager

ICON plc

Bangalore, India
Review site visit reports
Follow up on action items
Liaise between cra, ctm, pm
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

Job Summary

  • 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.
  • 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.
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

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.

Skills & Requirements

Must-have

  • Review site visit reports
  • Follow up on action items
  • Liaise between CRA, CTM, PM
  • Observe and escalate safety trends
  • Adhere to ICON's values
  • Process improvement focus

Nice-to-have

  • Foster an inclusive environment
  • Drive innovation and excellence
  • Shape the future of clinical development
  • Service oriented environment

Key Requirements

  • Bachelor’s degree in life sciences
  • Minimum 8-10 years Clinical Research experience
  • At least 5 years on-site monitoring experience
  • Experience in On-Site Monitoring
  • Experience in Clinical Trial Management
  • Thorough knowledge of ICH GCP
  • Fluent in written and spoken English

Work Rights

Not specified

Tailored Resume

Cover Letter