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Masterclass Certificate in Clinical Research Informatics

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๊ณผ์ • ์„ธ๋ถ€์‚ฌํ•ญ

  • Introduction to Clinical Research Informatics
  • Data Management in Clinical Trials (Clinical Data Management, CDISC)
  • Electronic Data Capture (EDC) Systems and Software
  • Clinical Trial Data Analysis and Reporting (Statistical Analysis, SAS Programming)
  • Regulatory Compliance and Data Governance in Clinical Research
  • Data Security and Privacy in Clinical Research (HIPAA, GDPR)
  • Big Data and Machine Learning in Clinical Research Informatics
  • Interoperability and Data Standards in Clinical Research (HL7, FHIR)

๊ฒฝ๋ ฅ ๊ฒฝ๋กœ

Clinical Research Informaticist Roles Description Clinical Data Manager (CDM) Oversees the collection, cleaning, and management of clinical trial data, ensuring data integrity and compliance.

High demand in pharmaceutical and CRO sectors.

Biostatistician Applies statistical methods to analyze clinical trial data, interpreting results and drawing meaningful conclusions.

Essential for study design and reporting.

Data Scientist (Clinical Research) Utilizes advanced analytical techniques and machine learning to identify patterns and insights from large clinical datasets.

Growing area of specialisation.

Programmer Analyst (SAS/R) Develops and maintains software programs for data management, analysis, and reporting.

Expertise in SAS or R is crucial.

Database Administrator (Clinical Research) Manages and maintains clinical databases, ensuring data security, accessibility, and optimal performance.

Critical for large-scale trials.

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์ƒ˜ํ”Œ ์ธ์ฆ์„œ ๋ฐฐ๊ฒฝ
MASTERCLASS CERTIFICATE IN CLINICAL RESEARCH INFORMATICS
์—๊ฒŒ ์ˆ˜์—ฌ๋จ
ํ•™์Šต์ž ์ด๋ฆ„
์—์„œ ํ”„๋กœ๊ทธ๋žจ์„ ์™„๋ฃŒํ•œ ์‚ฌ๋žŒ
London School of International Business (LSIB)
์ˆ˜์—ฌ์ผ
05 May 2025
๋ธ”๋ก์ฒด์ธ ID: s-1-a-2-m-3-p-4-l-5-e
์ด ์ž๊ฒฉ์ฆ์„ LinkedIn ํ”„๋กœํ•„, ์ด๋ ฅ์„œ ๋˜๋Š” CV์— ์ถ”๊ฐ€ํ•˜์„ธ์š”. ์†Œ์…œ ๋ฏธ๋””์–ด์™€ ์„ฑ๊ณผ ํ‰๊ฐ€์—์„œ ๊ณต์œ ํ•˜์„ธ์š”.
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