cra ii - Taipei, Taipei City

We're proud to foster an inclusive environment driving innovation and excellence, · and we welcome you to join us on our mission to shape the future of clinical development. · ...

We are currently seeking a Senior Clinical Research Associate II to join our diverse and dynamic team. As a Senior Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing ...

Sites monitoring and site management responsibility for clinical studies according to Company and/or Sponsor Standard Operating Procedures and Regulatory Guidelines. · ...

Taiwan-Homebased Senior CRAICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical develo ...

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory ...

Clinical Research Associate- Taiwan - Office Hybrid in ICON Taipei officeICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our ...

Roles within Clinical Monitoring/CRA are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centralized location. · ...

Syneos Health is seeking a CRA II for our FSP BU in Korea & Taiwan. The successful candidate will oversee clinical research studies by monitoring data and processes from a centralized location. · • Performs site qualification, site initiation, interim monitoring, site management ...

Work Schedule · Standard (Mon-Fri) · Environmental Conditions · Office · Essential Functions · Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and ...

Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. · ...

中國信託商業銀行Your Career Our Future · 【工作內容】 · 1.新興企業徵信報告撰寫 · 2.實地訪廠及風險揭露 · 3.協助業務端共同把關風險及架構案件 · 4.主管交辦事項 · 【資格條件】 · .工作經歷要求:具3年以上法金業務/徵信相關經驗 · .學歷要求:大學(含)以上,商管系所畢 · .證照條件:具備初階授信及初階外匯證照尤佳 · 【職缺資訊】 · .薪資待遇:面議(經常性薪資達4萬元或以上) · .職務屬性:全職 · .上班時段:日班,08:50~17:30 · .休假制度:依公司規定 · .工作地點:台北/新北/桃 ...

· 風險_新興徵信cra人員(全台) · 新興企業徵信報告撰寫 · 實地訪廠及風險揭露 · ...

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory ...

Job Overview · Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. · Essential Functions · Assist Clinical Research Associates (CRAs) and Reg ...

Job Overview · Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. · Essential Functions · • Assist Clinical Research Associates (CRAs) and R ...

Job Overview · Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. · Essential Functions · • Assist Clinical Research Associates (CRAs) and R ...

Assists in coordination and administration of clinical studies from the start-up to execution and closeout · Collects, assists in preparation, reviews and tracks documents for the application process. Assists in timely submission of proper application/documents to EC/IRB and, whe ...

ᴘᴜʀᴘᴏsᴇ ᴏғ ᴛʜɪs ᴘᴏsɪᴛɪᴏɴ · The role is an experienced cybersecurity testing engineer responsible for supporting product teams through structured security testing and compliance verification. The position ensures that product cybersecurity best practices are consistently adopted a ...

When our values align, there's no limit to what we can achieve. · At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something ...

The Site Care Partner acts as a Subject Matter Expert aimed to optimize country and site selection activities by proactively collaborating with key stakeholders and providing local intelligence to country outreach surveys, · Deploy GSSO site strategies by qualifying and activatin ...