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Certificate Programme in Drug Development Clinical Trials

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๊ณผ์ • ์„ธ๋ถ€์‚ฌํ•ญ

  • Introduction to Drug Development and Clinical Trials
  • Good Clinical Practice (GCP) and Regulatory Affairs
  • Clinical Trial Design and Methodology
  • Data Management and Statistical Analysis in Clinical Trials
  • Pharmacovigilance and Safety Reporting
  • Clinical Trial Project Management
  • Medical Writing and Communication in Clinical Trials
  • Case Study: A Comprehensive Clinical Trial (includes Drug Development and Regulatory processes)

๊ฒฝ๋ ฅ ๊ฒฝ๋กœ

Career Roles in Drug Development & Clinical Trials (UK) Description Clinical Research Associate (CRA) Oversee clinical trials, ensuring adherence to protocols and regulations.

High demand in the UK's thriving pharmaceutical sector.

Clinical Data Manager (CDM) Manage and analyze clinical trial data, ensuring accuracy and integrity.

Essential for effective drug development and regulatory submission.

Biostatistician Analyze clinical trial data using statistical methods.

Critical for interpreting results and informing drug development decisions.

Regulatory Affairs Specialist Navigate complex regulatory processes, ensuring compliance with UK and international regulations.

A crucial role in bringing new drugs to market.

Pharmacovigilance Specialist Monitor drug safety and report adverse events.

A vital role in protecting patient safety and ensuring drug safety post-market.

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์™œ ์‚ฌ๋žŒ๋“ค์ด ๊ฒฝ๋ ฅ์„ ์œ„ํ•ด ์šฐ๋ฆฌ๋ฅผ ์„ ํƒํ•˜๋Š”๊ฐ€

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๊ฒฝ๋ ฅ ์ธ์ฆ์„œ ํš๋“

์ƒ˜ํ”Œ ์ธ์ฆ์„œ ๋ฐฐ๊ฒฝ
CERTIFICATE PROGRAMME IN DRUG DEVELOPMENT CLINICAL TRIALS
์—๊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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