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Career Advancement Programme in Drug Safety Evaluation

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Drug Safety Evaluation: Advance your career in pharmacovigilance! This programme is designed for pharmacists, toxicologists, and medical professionals seeking career advancement in drug safety. Learn regulatory affairs, risk management, and clinical trial data analysis.

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์ด ๊ณผ์ •์— ๋Œ€ํ•ด

Develop crucial skills in signal detection and case reporting. Gain expertise in ICH guidelines and Good Pharmacovigilance Practices (GVP). Boost your resume and enhance your job prospects. Enroll today and unlock your potential in this vital field. Explore the programme details and secure your place now!

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์–ด๋””์„œ๋“  ํ•™์Šต

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์™„๋ฃŒ๊นŒ์ง€ 2๊ฐœ์›”

์ฃผ 2-3์‹œ๊ฐ„

์–ธ์ œ๋“  ์‹œ์ž‘

๋Œ€๊ธฐ ๊ธฐ๊ฐ„ ์—†์Œ

๊ณผ์ • ์„ธ๋ถ€์‚ฌํ•ญ

  • Principles of Drug Safety and Pharmacovigilance
  • Regulatory Requirements for Drug Safety
  • Case Report Form (CRF) Completion and Review
  • Signal Detection and Assessment
  • Risk Management Planning and Implementation
  • Data Analysis and Reporting in Drug Safety
  • Adverse Event Causality Assessment
  • Good Pharmacovigilance Practices (GVP)
  • Medical Writing and Communication in Drug Safety

๊ฒฝ๋ ฅ ๊ฒฝ๋กœ

Career Role (Drug Safety Evaluation) Description Pharmacovigilance Scientist Responsible for the detection, assessment, understanding and prevention of adverse effects or any other drug-related problem.

A key role in ensuring patient safety.

Drug Safety Physician Medical expert in drug safety, leading the assessment and management of safety signals and contributing to regulatory submissions.

High-level expertise in risk management.

Safety Data Manager Manages and analyzes large datasets of safety information, ensuring data quality and integrity for regulatory reporting.

Critical for compliance.

Regulatory Affairs Specialist (Drug Safety) Navigates the complex regulatory landscape, ensuring compliance with global safety standards and interacting with regulatory agencies.

Focus on submission and compliance.

Clinical Safety Associate/Scientist Supports the drug safety team in various tasks, contributing to safety assessments and regulatory reporting.

Entry-level to mid-level career progression.

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์‚ฌ์ „ ๊ณต์‹ ์ž๊ฒฉ์ด ํ•„์š”ํ•˜์ง€ ์•Š์Šต๋‹ˆ๋‹ค. ์ ‘๊ทผ์„ฑ์„ ์œ„ํ•ด ์„ค๊ณ„๋œ ๊ณผ์ •.

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

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์ด ๊ณผ์ •์˜ ๋น„์šฉ์„ ์ง€๋ถˆํ•˜๊ธฐ ์œ„ํ•ด ํšŒ์‚ฌ๋ฅผ ์œ„ํ•œ ์ฒญ๊ตฌ์„œ๋ฅผ ์š”์ฒญํ•˜์„ธ์š”.

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์ƒ˜ํ”Œ ์ธ์ฆ์„œ ๋ฐฐ๊ฒฝ
CAREER ADVANCEMENT PROGRAMME IN DRUG SAFETY EVALUATION
์—๊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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