Talaria
About the Role
• Perform Selection, Initiation, Monitoring and Close-out Visits at Sites according to project schedule.
• Adhere to project plans and applicable SOPs for monitoring requirements.
• Participate in feasibility and/or site identification activities if required.
• Collect regulatory documents and review these for accuracy and completeness.
• Train the site staff in the required trial-specific information and trial quality standard.
• Monitor at clinical study sites to assure adherence to GCP, SOPs, and study protocol.
Requirements
At least one year of independent clinical monitoring experience
Relevant Life science degree / Medical / Nurse / Pharmacology degree background
Excellent communication skills in English, both written and verbal
Computer literate and proficient in Microsoft Office.
Excellent interpersonal and organisationals skills.
Demonstrated ability to work independently and to effectively prioritise tasks.
About the Company
Talaria (former Gaea APAC Inc.) established 2021, a proud member of Gaea OU.
by demanding new ear renamed and reorganized team for specialized for clinical trial management.
Based on the Seoul, South Korea, one of Top 10 clinical trial region.
expand our coverage field to Asia Pacific and world wide.
Specialized Adverse Event assessment algorithm and software program were developed got patent from Korean Intellectual Property Office (KIPO) on 2023. we are leading Independent Data Monitoring Committee (IDMC) in clinical trial.