Centralized Clinical Trial Manager
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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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