PSI CRO Verified 9h ago
Pharmacovigilance Coordinator (Japanese Skills Required)
Prague, Prague, Czechia Hybrid
Salary not listedPaySalary not listed
TypeFull-time
Work settingHybrid
Verified listing
JobFig found this opening at its original source and checks that it remains available.
About the role
We are looking for a knowledgeable and proactive Pharmacovigilance Coordinator to join our enthusiastic and vibrant team. In this role, you will provide day-to-day support to the company’s global Pharmacovigilance Department and In-country Clinical Caretaker (ICCC) in clinical trials with the corresponding services. You will process and report safety information (including electronic reporting) throughout the course of the clinical trials. You will help to enhance patient care and safety in relation to the use of novel pharmaceuticals and investigational devices, collect relevant and reliable medical scientific information.
What you'll bring
- College or University Degree
- Full working proficiency in English and Japanese
- Administrative work experience
- Organizational and planning skills
- Detail-oriented, able to multi-task and work in a fast-paced environment
- Communication and collaboration skills
- Proficiency in standard MS Office applications (Word, Excel and PowerPoint)
- At least 1-year prior experience in Clinical Research as a Clinical Trial Coordinator or similar clinical operational role, Pharmacovigilance Coordinator, Regulatory specialist, Data Management Specialist or the like will be a plus
- Experience with safety databases and E2B reporting to regulatory authority in Japan (PMDA) and other regulators is a plus
- Biology, Bioscience, or Pharmacy is preferred