爱恩康欢迎最新从事过医学编码等行业的优秀人才加入我们，爱恩康临床医学研究（北京）有限公司将为您提供广阔的发展平台！
PRIMARY FUNCTION
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？ Responsible for ensuring the completeness, accuracy, timeliness, quality and integrity of the Clinical
Trial Medical Coding tasks. Ensure data quality and consistency per applicable regulatory
requirements, SOP(s), Processes and data standards. Works with the project team to meet the study
objectives.
MAJOR RESPONSIBILITIES AND DUTIES
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？ Ensure all data management activities to be compliance with GCP, relevant regulatory requirements
and SOP/WI (work instructions) of Hutch-Med.
？ Ensure following and applying CDISC or applicable standard through Clinical Trail.
？ Follow and keep compliance with Hutch-Med SOPs, work instructions to be knowledgeable in
applicable sections as bellows, but limited to:
？ A. Create and Maintain Dictionary Coding Conventions;
？ B. Setup and perform dictionary coding in clinical trials;
？ C. Perform independent QC of coding process;
？ D. Managing Medical Dictionaries at function level;
？ Ensure acknowledge, follow and to be consistent with Hutch-Med Policies and procedures.
？ Update technical skills and knowledge for continuous enhancement of work.
Minimum Requirements:
？ Educated to at least Bachelor level in Medicine, Pharmacy, Biological Sciences, or health care
related disciplines.
？ For coder, at least 1 years’ experience working in medical coding
？ For Sr Coder, at least 5+ years’ experience working on clinical trial medical coding and its
application.
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