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Centralized Clinical Trial Manager

ICON plcElectronic City, BangalorePosted 5 months ago
  • Lead or staff
  • Hybrid
  • Full time
  • 8 to 10 years
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About the role

ICON conducts clinical research to help bring medicines and treatments to patients. This role reviews clinical trial visit reports, follows up on issues, and escalates safety and quality concerns.

What you'll do

  • Review and approve clinical trial visit reports
  • Follow up on action items and protocol deviations
  • Monitor trial metrics and report timelines
  • Escalate safety trends, outstanding issues, and risks to trial delivery
  • Attend project meetings and suggest quality improvements

Skills

Must have

  • Clinical trial management
  • Clinical research
  • On-site monitoring
  • Clinical trial data review
  • Ich GCP

Tools

  • Omr
  • Ico trial
  • Ctms

Who it's for

Education
Bachelor's degree
Degree
life sciences, healthcare
Experience
8 to 10 years
Languages
english
Domain
clinical research

About ICON plc

ICON plc has 27 open roles in Bangalore, at ICON plc Bengaluru. See every ICON plc role.

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