Clinical Project Coordinator/Clinical Trial Assistant - Taipei

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 ...

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 ...

We are 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 compliance wi ...

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 ...

We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. · ...

We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successful completion of clinical trials. · ...

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 ...

Join Us as a Clinical Trial Coordinator – Make an Impact at the Forefront of Innovation. · ...

About Ubiquiti · At Ubiquiti Inc., we create technology platforms for Businesses, Smart Homes, and Internet Service Providers, · driven by our goal to connect everyone, everywhere. · Design Stamping stage die & progressive tooling by CAD software independently. · ,Familiar with t ...

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 currently seeking a Manager, Clinical Operations to join our diverse and dynamic team. · Leading the operational planning and execution of clinical trials, · Engaging with cross-functional teams to optimize trial design and enhance operational efficiency throughout the cli ...

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, · ...

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 Field Application Specialist will be responsible for offering overall product expertise, application knowledge and technical support along each step of the customer process. The main mission is to ensure successful application, implementation, qualification, and use of our pr ...

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

The Clinical Data Associate reports to the Biometrics Project Manager on projects. · ...

We are seeking committed, skilled, and customer-focused individuals to join our winning team as a Clinical Trial IWRS Monitor for our Brightech location in Taipei, Taiwan with opportunities to work remotely in accordance with our Work from Home policy. · ...

+ Precision Medicine is not your typical CRO. · + The Project Support Specialist serves as a member of the project team providing cross-functional support with the goal of contributing toward efficient management of the studies to which they are assigned. · + Essential functions ...

We are currently seeking a Senior Statistical Programmer (all levels) to join our diverse and dynamic team. · Developing and validating SAS programs for statistical analysis and reporting of clinical trial data. · Collaborating with biostatisticians to define analysis plans and s ...

Job summary · We are currently seeking a Manager, Statistical Programming to join our diverse and dynamic team. As the Manager of Statistical Programming at ICON, you will lead a team of statistical programmers in the development and validation of statistical analysis and reporti ...