Centralized Clinical Trial Manager

ICON Clinical Research, LP

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

Job Summary

  • The role involves effectively reviewing site visit reports to ensure the highest standards of quality and minimize errors.
  • Candidates will act as a liaison between CRAs, Centralized 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 standards of quality and minimize errors.

Salary

Not specified; Competitive salary mentioned; Benefits include health insurance and retirement planning

Skills & Requirements

Must-have

  • Review site visit reports per protocol
  • Follow up on action items and deviations
  • Liaise between CRA, CTM, and PM
  • Escalate safety trends and issues
  • Ensure report quality and consistency
  • Monitor OMR and ICO trial metrics

Nice-to-have

  • Process improvement culture
  • Strong analytical skills
  • Collaborative team environment
  • Service-oriented mindset
  • Continuous improvement focus

Key Requirements

  • Bachelor's degree in life sciences or healthcare
  • 8-10 years clinical research experience
  • 5+ years on-site monitoring experience
  • Thorough knowledge of ICH GCP regulations
  • Fluent written and spoken English

Work Rights

Not specified

Tailored Resume

Cover Letter