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Seoul
Permanent
We are currently looking for talented Clinical Research Associates for our sponsor-dedicated position in Korea. We are proud to have an excellent team of the best professionals on the market and are looking for people who are ready to show true performance and interest in Clinical Trials. As a Clinical Research Associate you will lead all aspects of study site monitoring according to Covance SOP, ICH guidelines and GCP and you will take part in pre-study qualification and initiation visits, routi
8/11/2022 10:59:31 PM
Essential Job Duties: - Collect, track and perform a quality review of all essential & investigator documents required for effective and compliant study site activation and maintenance - - Ensure that all assigned maintenance and Start-up activities are on track and in accordance with client expectations, ICH/GCP, SOPs, budget, quality and applicable laws and guidelines Serve as primary contact for investigative sites and ensure documents required are collected in a timely manner. - Proactively m
8/10/2022 1:21:11 AM
The In-House Clinical Research Associate II (IHCRA II) is an essential member of a Clinical Project Team responsible for the execution of a Clinical Research Project. The degree of responsibility given to the IHCRA II shall reflect their experience, and level of contribution which they can make to the project. The work will involve Clinical Operations activities which will be conducted in an office or home based setting for designated projects as well as some travel to conduct site visits or to a
8/09/2022 7:57:45 AM
These are the specific areas of accountability requiring decisions or delivery of results. Most positions have between six to ten key job duties. In this section, list and describe the position's principal responsibilities in concise, but comprehensive statements. Include those accountabilities that are critical to the successful performance of the job. Indicate % of time in a single work week spent on top 5-10 duties (no less than 5% increments). ? Collect, track and perform a quality review of
8/08/2022 10:35:29 PM
LabCorp? ? ? ? ? ? ? Global Top tier CRO?, ? ? ? ? ? ? ? 6? ? ? ? ?. LabCorp?Global CRO ? ? ? Spectrum, ? ? ? Commercial ? Full service? ? ? ? ? CRO?. ? 2005? Legal entity ? ? ? 1? 4? ? indication ? ? ? ?, ? ? ? ? ? ? ? ? ? ? ? ? ? ?. Responsibilities include, but are not limited to: - Develops strong site relationships and ensures continuity of site relationships through all phases of the trial - Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SO
8/08/2022 7:44:29 AM
The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Covance, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Sr CRA II assures the implementation of project plans as assigned, functions as leader for projects of limited scope, as assigned and assumes line management responsibilities, as assigned. Acts in the project role of a Local Project Coordinator or Lead CR
8/08/2022 7:42:17 AM
Our HR Business Partners are integral to the success of our business and partner with our clinical operations team to aid them with human resource (HR) advice and assistance to ensure our employee experience is at the highest standard. The position is based at the office in Seoul South Korea. Joining us as the HR Business Partner for South Korea you will: Build strong working relationships, underpinned by trust, credibility and respect with business supervisors Seek to understand business strateg
8/07/2022 10:20:44 PM
8/07/2022 8:23:12 PM
Assist in or complete per the Safety Management Plan (SMP) the processing of all adverse event reports from any source. Assist in producing queries of safety data for clients as appropriate. Assist in the generation and maintenance of the PSS metrics. Assist Data Management or clients on reconciliation of safety databases. Provide input for monthly status reports. Maintains a comprehensive understanding of Standard Operating Procedures (SOPs), Work Instructions (WI), guidance documents and direct
8/07/2022 1:28:37 AM