You will contribute to site start-up and activation activities, taking responsibility for your deliverables and working collaboratively
Job Summary
You will contribute to site start-up and activation activities, taking responsibility for your deliverables and working collaboratively.
Leading the preparation and submission of regulatory documents, including clinical trial applications, ethics committee submissions, and regulatory agency communications.
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 contribute to site start-up and activation activities, taking responsibility for your deliverables and working collaboratively.
Skills & Requirements
Must-have
Regulatory document preparation and submission
Stakeholder coordination and liaison
Record management for submissions
Guidance on regulatory requirements
Process improvement initiatives
Nice-to-have
Fostering an inclusive environment
Driving innovation and excellence
Advancing innovative treatments and therapies
Key Requirements
Bachelor's degree in life sciences or related field
Minimum 2 years experience in clinical research
Specific experience in study start-up activities
Strong understanding of ICH-GCP
Excellent organizational and project management skills