Senior Global Regulatory Scientist
ICON plcElectronic City, BangalorePosted 19 days agoA free account shows the apply link for every role and matches you to the ones that fit your resume.
About the role
ICON is a global healthcare intelligence and clinical research organisation that supports the development of medicines and treatments. This scientist will lead regulatory work for clinical trial projects, including submission strategy, documentation, coordination, and client communication.
What you'll do
- Develop global clinical trial submission strategies
- Prepare and review regulatory plans and core documents
- Coordinate submissions to regulatory agencies and ethics committees
- Track submission progress and maintain accurate study records
- Manage regulatory study budgets and contracted scope
- Perform quality control reviews of regulatory deliverables
Skills
Must have
- Clinical trial regulatory submissions
- Regulatory strategy
- Regulatory planning
- Ich
- GCP
- Quality control
Tools
- Clinical trials management system
- Etmf
Who it's for
- Education
- Bachelor's degree
- Degree
- science
- Experience
- 3 to 6 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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