Welcome page Returning Candidate? Log back in! Clinical Safety Coordinator - Pharmacovigilance / Drug Safety Job Locations Taiwan-Taipei | Taiwan-Taipei Category Clinical Safety Job Summary

We are currently seeking a full-time, office-based Clinical Safety Coordinator to join our team in Taiwan office. This role is a vital part of the team to accomplish tasks and projects that are instrumental to the company’s success. If you are interested in an exciting career where you can use your expertise, develop and grow your career even further, then this is the opportunity for you.

Responsibilities

Working closely with the Clinical Safety Manager to ensure each project deliverables are met;

Collect, process, and track serious adverse event (SAE) reports and clinical event documents;

Generate and track study report safety narratives;

Coordinate safety surveillance activities (e.g., lab review and trend analysis);

Generate Investigator Safety Letters and distribution to health authority;

Assist in preparation of clinical safety documents 

Perform safety submissions of expedited/periodic reports in Singapore/Taiwan/China Qualifications

Bachelor’s degree in health/life sciences with 2-4 years of clinical trial safety or Pharmacovigilance experience ;

Proficient in a range of Clinical Safety tasks, as detailed in the ‘responsibilities’ section (above)

Excellent time management skills with an ability to work on tight timelines;

An ability to interact well within a team environment, but also work independently and manage own workload;

Proficient in Microsoft Office and demonstrated ability to efficiently use safety database;

Strong attention to detail;

Demonstrate comprehensive knowledge of Good Clinical Practice (GCP) guidelines

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

 

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

 

Medpace Perks

Hybrid work-from-home options (dependent upon position and level)Competitive PTO packagesEmployee health and wellness initiativesFlexible work scheduleCompetitive compensation and benefits packageStructured career paths with opportunities for professional growth

Awards

Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

 

 

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

 

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