Not specified; competitive within country; various...
Fully remote
Bachelor's degree in life sciences
Strong attention to detail
Excellent communication skills
This role plays a pivotal part in facilitating the initiation of clinical trials while ensuring compliance with regulatory requirements
Job Summary
This role plays a pivotal part in facilitating the initiation of clinical trials while ensuring compliance with regulatory requirements.
The successful candidate will assist in preparing and submitting regulatory documents such as clinical trial applications and ethics committee submissions.
ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a culture focused on inclusion and belonging.
Matching Summary
This role plays a pivotal part in facilitating the initiation of clinical trials while ensuring compliance with regulatory requirements.
Salary
Not specified; Competitive within country; Various annual leave entitlements; Health insurance offerings; Retirement planning offerings
Skills & Requirements
Must-have
Bachelor's degree in life sciences
Strong attention to detail
Excellent communication skills
Ability to work independently
Nice-to-have
Previous clinical research experience
Regulatory affairs background
CMC experience
Collaborative cross-functional teamwork
Key Requirements
Bachelor's degree in life sciences or related field
Location: South Korea (Home-based)
Experience in clinical research preferred but not required