Clinical Research Associate II
HybridSeoul, Seoul, South Korea
Job Summary
Conduct onsite monitoring visits, manage study startups, and perform CRF reviews with source verification and query resolution. Facilitate site budgets and contract negotiations while monitoring trial progress at the country level. Build relationships with clinical sites and investigators, acting as a point of contact for in-house support services and vendors. Communicate with internal project teams regarding study progress and participate in feasibility research. Support the regulatory team in preparing documents for study submissions. Ensure subject rights, safety, and data compliance across full-service global projects in South Korea.
Required Qualifications
- College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience
- Independent on-site monitoring experience in Korea
- Experience in all types of monitoring visits in Phase II and/or III
- Full working proficiency in English and Korean
- PC skills to be able to work with MS Word, Excel and PowerPoint
- Ability to plan, multitask and work in a dynamic team environment
- Communication, collaboration, and problem-solving skills
- Ability to travel
Desired Qualifications
- Experience in feasibility assessment and study set-up process is preferable
- Experience in Multiple Sclerosis, Inflammatory Bowel Disease, Oncology, Infectious Diseases is a plus
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