PSI CRO is hiring a

Clinical Research Associate II

Seoul, South Korea
Full-Time

We’re searching for a knowledgeable, team-oriented CRA II to manage the clinical aspects of full-service global projects in South Korea, Seoul. As a CRA II at PSI, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators.  You will focus on subjects’ rights, safety and well-being and quality of data compliance.

Office-Based in Seoul, South Korea

You will:

  • Conduct and report all types of onsite monitoring visits
  • Be involved in study startup
  • Perform CRF review, source document verification and query resolution
  • Facilitate site budgets and contract negotiations
  • Monitor trial progress on the country level
  • Be responsible for site communication and management
  • Be a point of contact for in-house support services and vendors
  • Communicate with internal project teams regarding study progress
  • Participate in feasibility research
  • Support regulatory team in preparing documents for study submissions

 

  • 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
  • Experience in feasibility assessment and study set-up process is preferable
  • Experience in Multiple Sclerosis, Inflammatory Bowel Disease, Oncology, Infectious Diseases is a plus
  • 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

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

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