Senior Clinical Research Associate - Taipei, Taipei City

We are looking for a talented and highly motivated Research Associate to join the Ochre Bio Team in TPE on an exciting journey to support the development of advanced RNA medicines for one of the most pressing healthcare challenges of our time. · Ochre's Taipei site is a highly un ...

· HSBC Securities Taiwan is a full licensed securities house with focus on cash equity brokerage business in Taiwan. · HSBC Global Investment Research (GIR) is a 'CIB client servicing and revenue generating' global business unit, positioned as one of the key business lines of CI ...

Responsibilities · Support senior analysts in conducting fundamental research across technology-related industries · Assist in forming global research perspectives and identifying long-term sector trends · Perform company/industry data collection, channel checks, and structured r ...

Job Overview · Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. · Essential Functions · • Perform site monito ...

Job Overview · Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. · Essential Functions · Perform site monitori ...

Job Overview · Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. · Essential Functions · • Perform site monito ...

Taiwan-(Senior) CRA (Oncology) -Client office based with Flexible WFHICON 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 miss ...

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 ...

Primarily responsible for coordinating the various aspects of clinical trials. Works as part of a clinical delivery team providing support, guidance and advice on a local level. Develops existing tools and processes to identify areas of improvement and ensures business continuity ...

職務說明 · Be responsible for initiating, organizing and managing the assigned studies. · On site monitoring and site managements for global studies. · Ensure clinical trials conducted in compliance with protocol & GCP. · Ensure clinical trials can be conducted per timeline requireme ...

Job Description · Support Clinical Operation Assistant (COA) on tasks (such as administrative work) · Training will be provided through intern period to enhance intern's understanding of CRO industry. · Education · New graduate with recent Bachelor or master's degree in nursing, ...

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 ...

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, · regula ...

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

Act as PAREXEL's direct contact with assigned sites. · Build relationships with investigators and site staff.Facilitate and support site with access to relevant study systems. · ...

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 ...

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 Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. · Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. · Conducting site visits to ass ...

The Senior Clinical Research Associate will be responsible for monitoring progress of clinical studies at the site level to verify that the rights and well being of subjects are protected... · Bachelor's degree or equivalent required in life sciences. · Requires at least 5 years ...

This role is for a Senior Clinical Research Associate as a Lead Monitor responsible for compliance and oversight of clinical trials that implement a Risk-Based Monitoring (RBM) strategy. · Develop and execute monitoring plans through protocol analysis for remote risk management. ...