You will be instrumental in ensuring the transparency and integrity of clinical trial data and results
Job Summary
You will be instrumental in ensuring the transparency and integrity of clinical trial data and results.
You will be responsible to plan, lead and coordinate activities for submissions documents related to redaction/anonymization activities for Health Canada PRCI and EMA Policy 0070.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.
Matching Summary
You will be instrumental in ensuring the transparency and integrity of clinical trial data and results.
Skills & Requirements
Must-have
Clinical trial transparency regulations
Health Canada PRCI
EMA Policy 0070
Document anonymization
Regulatory reporting
Nice-to-have
Fostering an inclusive environment
Driving innovation and excellence
Shaping the future of clinical development
Stakeholder management skills
Key Requirements
Advanced degree in relevant field
Extensive experience in clinical trial transparency