Summary
Location
Tokyo
Type
full-time
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About this role
We are currently seeking a full-time, office-based Drug Safety Coordinator/Safety Specialist to join our Clinical Safety department in Tokyo, Japan. This position will be focused on the handling and processing of adverse events from all sources, including clinical trials and post marketing surveillance.
Responsibilities
- Determine plan of action for incoming calls;
- Collect, process, and track incoming events;
- Write safety narratives;
- Report on various safety data; and
- Collaborate with internal departments and investigative clinical research sites to ensure compliance with safety processes.
Qualifications
- Bachelor's of Science in Nursing;
- At least one year of clinical experience;
- Clinical Research/Post marketing Pharmacovigilance experience is preferred;
- Proficient knowledge of Microsoft® Office;
- Broad knowledge of medical terminology;
- Strong organizational and communication skills.
- Bilingual Japanese and English
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 6,000 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
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with opportunities for professional growth
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Awards
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually 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.
Other facts
About Medpace, Inc.
Medpace is a scientifically-driven, global, full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Medpace’s mission is to accelerate the global development of safe and effective medical therapeutics through its high-science and disciplined operating approach that leverages local regulatory and deep therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs approximately 6,000 people across 44 countries.
What you'll do
- The Clinical Safety Coordinator will handle and process adverse events from various sources, including clinical trials and post-marketing surveillance. Responsibilities include determining action plans for incoming calls, collecting and tracking events, writing safety narratives, and ensuring compliance with safety processes.
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