Centralized Clinical Trial Manager

ICON plc

Bangalore, India
Not specified; competitive salary mentioned; vario...
Review site visit reports per protocol
Follow up on action items and deviations
Liaise between cra ctm and pm teams
The role involves effectively reviewing site visit reports to ensure the highest quality standards and minimize errors

Job Summary

  • The role involves effectively reviewing site visit reports to ensure the highest quality standards and minimize errors.
  • Candidates must act as a liaison between CRAs, Clinical Trial Managers, and Project Managers to resolve issues timely.
  • ICON offers competitive benefits including health insurance, retirement planning, and a global employee assistance program.

Matching Summary

The role involves effectively reviewing site visit reports to ensure the highest quality standards and minimize errors.

Salary

Not specified; Competitive salary mentioned; Various annual leave entitlements and health insurance offered

Skills & Requirements

Must-have

  • Review site visit reports per protocol
  • Follow up on action items and deviations
  • Liaise between CRA CTM and PM teams
  • Escalate safety trends in patients
  • Thorough knowledge of ICH GCP regulations

Nice-to-have

  • Strong analytical skills for data review
  • Process improvement culture mindset
  • Excellent written and spoken English
  • Ability to collaborate across diverse teams
  • Willingness to travel if required

Key Requirements

  • Bachelor's degree in life sciences or related field
  • 8-10 years of Clinical Research experience
  • At least 5 years of on-site monitoring experience
  • Proficiency in OMR ICO trial systems
  • Fluent in written and spoken English

Work Rights

Not specified

Tailored Resume

Cover Letter