Clinical Site Associate - Taipei, Taipei City

We are currently seeking a Site Management Associate I to join our diverse and dynamic team. As a Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites by assisting with site monitoring activities, ensuring compl ...

Clinical Site 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 mis ...

We are currently seeking a Site Management Associate I to join our diverse and dynamic team. · To be successful in this role you will assist with site monitoring activities, ensure compliance with study protocols and maintain high standards of operational efficiency. You will con ...

Key Accountabilities · Oversight of Monitoring Responsibilities and Study Conduct : · Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and qual ...

We are currently seeking a Site Management Associate (SSU Associate) to join our diverse and dynamic team. · ...

We are currently seeking a Site Management Associate I to join our diverse and dynamic team. As a Site Management Associate I at ICON, you will play an important role in supporting the management of clinical trial sites by assisting with site monitoring activities, ensuring compl ...

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 ...

Clinical Research Associate II- ICON Taiwan office Hybrid · ICON 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 sh ...

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 ...

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 R ...

Key Responsibilities · Partner Acquisition and Pipeline Development · Identify, evaluate, and onboard channel partners in priority categories (e.g., · P&A/Industrial, Luxury/Collectibles). · Build and manage a structured acquisition pipeline; collaborate closely with our sole · a ...

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 tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include ...

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

Taiwan-CRA-all level (All program) · ICON 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 clini ...

Job Overview · Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include ...

The Clinical Study Administrator is responsible for contributing to site activation by assisting with site staff access to vendor systems and following up with sites to ensure training completion. They also coordinate the Investigator’s Site File printing and shipment to sites as ...

We are Covestro. We refine chemical material solutions with game-changing products. · Join us and our colleagues now and together we will make the world a brighter place. · Provide high-level management assistance to the Managing Director of both legal entities, ensuring timely a ...

This role is focused on delivering technical support to CEM service providers. · Candidate Profile · Experience in manufacturing test of advanced HPM and server systems. · Thorough understanding of the fundamentals of electronics. · ...