Senior CRA - Beijing, Beijing

ICON plc is a world-leading healthcare intelligence and clinical research organization.We are seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team.We're proud to foster an inclusive environment driving innovation and excellence. · ...

We are seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team.We're proud to foster an inclusive environment driving innovation and excellence. · ...

ICON plc is seeking a Senior Clinical Research Associate (CRA) to oversee and manage clinical trial activities in Beijing.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 criti ...

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 hiring CRA I for Parexel Core. · To perform clinical monitoring activities of designated projects in accordance with the Parexel's SOPs (or the Sponsor's SOPs as appropriate), which include: investigator/site selection, managing and coordinating site related activities, co ...

We're proud to foster an inclusive environment driving innovation and excellence, · Monitoring clinical trial sites to ensure adherence to study protocols, · Conducting site visits to assess site performance, · Collaborating with cross-functional teams,Various annual leave entitl ...

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 ...

The Senior CRA I is responsible for site monitoring and site management. · The role involves implementing project plans, leading projects of limited scope, assuming line management responsibilities, · and acting in the project role of a Local Project Coordinator or Lead CRA as as ...

The CRA I is responsible for site monitoring and management of clinical studies. They ensure the implementation of project plans, perform routine monitoring and closeout of clinical sites, maintain study files, conduct pre-study and initiation visits, liaise with vendors, and oth ...

Responsable por la supervisión del sitio clínico según las directrices establecidas por la empresa o patrocinador. · Implementar planes de proyecto asignados. · Mantener archivos estudiando, realizar visitas previas al estudio e iniciación, coordinar con proveedores, entre otros. ...

Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. · Responsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sit ...

This position involves deducing clinical trends and differentiations from clinical designs and data read-outs. · Monitoring and collecting secondary information from various sources such as clinical databases. · Assisting in data preparation, deliver components of projects, and e ...

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. · A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the front-line of medical ...

We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. · In short, to be the partner of choice in drug development. That's our vision. ...

We are seeking a Research Consultant to join our team. · The successful candidate will be responsible for deducing clinical trends, monitoring secondary information from various sources, and conducting market research with senior support. · Deduce clinical trends, differentiation ...

This Clinical Quality Assurance Manager position involves overseeing quality assurance activities for clinical studies. · ...

This senior leader will establish and lead a dedicated Site Management Unit (SMU) within a clinical research environment in China. · Bachelor's degree in Life Sciences or related field; advanced degree preferred · 10–15 years of experience in clinical research with strong backgro ...

The Clinical Quality Assurance (CQA) Manager is responsible for leading QA activities to ensure high-quality data and compliance with regulatory requirements. · Key responsibilities include:Developing and implementing quality assurance plans for clinical trials. · Conducting audi ...

The Clinical Quality Assurance Manager is responsible for making annual QA plans for study audit and system audit, providing feedback and recommendations to study site staff, and conducting root cause analysis on significant inspection and audit findings. · ...

Department: APAC (In-Market) · Employment Type: Full Time / Term (3-year fixed term contract) · Language Designation: Bilingual – English and Mandarin · Posting Close Date: March 8, 2026 · About Destination Canada · Tourism is the heartbeat of communities from coast to coast to c ...