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Drug Safety Associate (4-Month Contractor)

1-3 years
Not Disclosed
10 July 18, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Drug Safety Associate (4-month Contract) – ICON plc – Taipei

Job Summary:
ICON plc, a global clinical research and healthcare intelligence leader, is hiring a Drug Safety Associate (Contractor) in Taipei, Taiwan. This 4-month project position supports pharmacovigilance activities including AE reporting, regulatory compliance, and safety data management across a range of study types. Ideal for healthcare professionals or study coordinators seeking pharma experience, this role offers hybrid flexibility and global exposure within a high-performance CRO environment.


Key Responsibilities:

  • Collect, translate, transcribe, and enter adverse event (AE) data from various sources into safety databases

  • Manage timely reporting and distribution of safety documents (SAE, SUSAR, DSUR, PSUR)

  • Ensure compliance with local health authority (LHA) regulations and internal SOPs

  • Collaborate with global Patient Safety teams to analyze and escalate safety data

  • Maintain accurate and updated safety databases and filing systems

  • Support audits, CAPAs, and health authority inspections

  • Monitor local pharmacovigilance regulations and implement necessary updates

  • Prepare KPIs and root-cause analysis for delayed reports

  • Review safety sections in Phase IV/NIS protocols and coordinate with CROs as needed

  • Conduct training for internal teams and external partners on AE reporting processes


Required Skills & Qualifications:

  • Degree in a healthcare-related field (nursing, pharmacy, medicine, etc.)

  • Proficiency in English and Mandarin (written and spoken)

  • Knowledge of pharmacovigilance regulations (local and global)

  • Understanding of pharmacological and medical terminology

  • Excellent interpersonal, communication, and problem-solving skills

  • Experience with safety databases and documentation systems

  • Study coordinators with relevant background are encouraged to apply


Perks & Benefits:

  • Competitive salary for short-term contract role

  • Hybrid work setup with flexibility to work from home

  • Health insurance options for contractor duration

  • Access to Global Employee Assistance Programme (TELUS Health)

  • Local benefits may include transport subsidies, gym discounts, and wellness programs

  • Inclusive and collaborative global work culture


About ICON plc:

ICON plc is a leading global Contract Research Organization (CRO) delivering advanced clinical research solutions across all therapeutic areas. With a presence in over 40 countries, ICON is known for its innovation in pharmacovigilance, drug development, and healthcare intelligence.


Work Mode: Hybrid – Based in Taipei, Taiwan (client office with WFH flexibility)


Call to Action:

Looking to grow your pharma safety career with a global CRO? Apply today for this 4-month contract role with ICON and contribute to safer healthcare outcomes worldwide.