Not specified; competitive salary mentioned; vario...
Bachelor's degree in life sciences
2 years clinical research experience
Study start-up activities expertise
The role involves leading the preparation and submission of regulatory documents including clinical trial applications and ethics committee submissions
Job Summary
The role involves leading the preparation and submission of regulatory documents including clinical trial applications and ethics committee submissions.
ICON fosters an inclusive environment driving innovation and excellence while shaping the future of clinical development.
The company offers competitive benefits including health insurance, retirement planning, and a global Employee Assistance Programme.
Matching Summary
The role involves leading the preparation and submission of regulatory documents including clinical trial applications and ethics committee submissions.
Salary
Not specified; Competitive salary mentioned; Various annual leave entitlements included
Skills & Requirements
Must-have
Bachelor's degree in life sciences
2 years clinical research experience
Study start-up activities expertise
ICH-GCP regulatory knowledge
Local regulatory requirements understanding
Nice-to-have
Process improvement initiative participation
Cross-functional team collaboration skills
Strong organizational abilities
Excellent communication skills
Key Requirements
Bachelor's degree in life sciences or related field