Clinical Research Associate I/II [South Korea]


 
Company Description


We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the front-line of medical science, changing lives, and bringing new medicines to those who need them.

If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you.


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Job Description


As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

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
  • 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
  • Participate in quality control and compliance monitoring
  • Support regulatory team in preparing documents for study submissions

Qualifications
  • College/University degree in Life Sciences, Pharmacy, RN or an equivalent combination of education, training & experience
  • Independent on-site monitoring experience in Korea
  • At least 1 year of independent on-site monitoring experience in Korea for CRA I
  • At least 3 years of independent on-site monitoring experience in Korea for CRA II
  • 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 Oncology or Hematology therapeutic indications is a plus (preferable)
  • 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

Additional Information


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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