Regulatory Manager

Our ideal candidate will possess:


Tertiary qualifications in related science or health care discipline
At least 8 years’ experience in clinical research environment
Demonstrated experience interacting with Health Authorities in South Korea
Extensive knowledge of clinical trial related regulatory requirements in South Korea
Comprehensive understanding of regulatory reporting requirements in South Korea
Strong knowledge of ICH and GCP guidelines
Fluent in English and Korean
Experience in mentoring and motivating colleagues to accomplish tasks
Excellent communication and networking skills with key stakeholders
Excellent presentation and interpersonal skills
Strong problem solving, analytical skills and strategic thinking abilities
Well organized, good time management skills and ability to prioritise


Our ideal candidate will be located in Seoul with full working rights in South Korea.

You must have an excellent track record in working in South Korea in order to be considered for this role.

This is an excellent opportunity to work with a growing and global CRO.