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Medpace

Global CRO delivering full-service clinical trials

Project Assistant - Clinical Safety

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeTaipei City, TaiwanNo salary listed

About the Job

Requirements

  • A bachelor's degree or above is required.
  • Fluency in English and Mandarin is required.
  • Proficiency in Microsoft Office is required.
  • Strong organization and task prioritization skills are required.
  • Strong attention to detail and strong oral and written communication skills are required.

Responsibilities

  • Support the Clinical Safety department by processing safety reports; creating and distributing safety notification letters; and tracking and filing correspondence with regulatory authorities, local ethics committees, sites, and GCP offices.
  • Prepare reports, presentations, agendas, correspondence, and meeting minutes as needed.
  • Track, process, and organize safety-related documents.
  • Perform basic research, answer questions from internal or external parties, or identify potential issues for further investigation in support of Clinical Safety department processes.
  • Learn and perform tasks in accordance with assigned standard operating procedures and policies.
  • Conduct quality-control reviews of department documents as needed.
  • Maintain databases and spreadsheets to facilitate tracking and documentation of department activities.
  • Mentor and train less experienced project assistants as needed.
  • Perform other duties as assigned by the Clinical Safety department.

Desired Qualifications

  • Majors related to pharmacy or medicine are preferred.
  • Candidates with 1–2 years of project coordination or administrative experience, or basic clinical safety knowledge, will be given priority.

About the Company

Medpace

Global CRO delivering full-service clinical trials

Medpace is a global Contract Research Organization that provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device companies. It manages Phase I–IV trials from study design and regulatory submissions to monitoring, data management, biostatistics, and final reporting, using a single integrated team. A key differentiator is its ownership of integrated laboratories—global central labs, a bioanalytical lab, and imaging/ECG core labs—ensuring streamlined workflows and consistent data. Its physician-led, scientifically driven approach and single-vendor model aim to reduce sponsor oversight and help bring therapies to market efficiently, with operations in over 40 countries.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Cincinnati, OH
Founded
1992

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