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Clinical Safety Coordinator - Pharmacovigilance / Drug Safety

3+ years
Preferred by Comapny
12 Nov. 25, 2024
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Job Opening: Clinical Safety Coordinator - Pharmacovigilance / Drug Safety

Location: Taipei, Taiwan
Department: Clinical Safety
Job ID: 10259


Overview

Medpace, a globally recognized clinical contract research organization (CRO), is seeking a dedicated Clinical Safety Coordinator for its Taiwan office. This full-time, office-based role is pivotal in supporting clinical safety projects and ensuring compliance with regulatory standards.

If you’re passionate about contributing to the development of safe and effective therapeutics, this role offers opportunities for growth and impactful contributions to global healthcare.


Key Responsibilities

  • Collaborate with the Clinical Safety Manager to achieve project milestones.
  • Handle Serious Adverse Event (SAE) reports, including collection, processing, and tracking.
  • Draft and monitor study report safety narratives.
  • Conduct safety surveillance activities, such as laboratory reviews and trend analyses.
  • Prepare and distribute Investigator Safety Letters to health authorities.
  • Assist in developing and managing clinical safety documents.
  • Submit expedited and periodic safety reports in SingaporeTaiwan, and China.

Qualifications

  • Education:

    • Bachelor’s degree in health or life sciences.
  • Experience:

    • 2–4 years of experience in clinical trial safety or pharmacovigilance.
  • Skills & Knowledge:

    • Strong grasp of Good Clinical Practice (GCP) guidelines.
    • Proficient in Microsoft Office and safety database tools.
    • Attention to detail and ability to meet tight deadlines.
    • Team player with excellent time management skills.
    • Capable of working independently while managing multiple priorities.

Why Join Medpace?

Perks and Benefits

  • Flexible work environment.
  • Competitive salary and benefits.
  • Generous Paid Time Off (PTO) policy.
  • Structured career advancement opportunities.
  • Employee wellness initiatives and appreciation events.

Global Impact and Recognition

  • Over 30+ years of experience in advancing therapeutic solutions.
  • Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024).
  • Winner of multiple CRO Leadership Awards for expertise and reliability.

How to Apply

Interested candidates can apply for Job ID 10259 through the Medpace Career Portal.

Join Medpace and be part of a mission to transform global healthcare while advancing your career in clinical safety and pharmacovigilance.