Clinical Trial Assistant - Beijing

Clinical Trial Associate, Beijing, office based · 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 fu ...

We're proud to foster an inclusive environment driving innovation and excellence, · & we welcome you to join us on our mission to shape the future of clinical development. · Assist in the coordination and administration of clinical trials, · Maintain and organize clinical trial d ...

A Senior Site Manager serves as the primary contact point between the Sponsor and the Investigational Site. · ...

At Emerald Clinical Trials, we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia-Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, m ...

We are seeking a Clinical Trial Administrator to join our diverse and dynamic team.As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and analysis of clinical trials, interpreting complex medical data, and contributing to the adva ...

We are dedicated to advancing clinical research through scientific expertise and operational excellence. · ...

This role is responsible for providing administrative and clinical site payment support for clinical projects. · ...

We are a global, full-service Contract Research Organization (CRO) dedicated to advancing clinical research through scientific expertise and operational excellence. · We combine global reach with local knowledge to deliver better engagement, more accurate data, and faster results ...

A Site Manager serves as the primary contact point between the Sponsor and the Investigational Site. A Site Manager is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Cli ...

A Site Manager serves as the primary contact point between the Sponsor and the Investigational Site. · ,,Acts as primary local company contact for assigned sites for specific trials. · ,Maintains complete, accurate and timely data and essential documents in relevant systems utili ...

The Payment Specialist will provide administrative support for clinical projects contributing to their overall management. · Provide project support to the Clinical Site Payments team. · ...

A Site Manager serves as the primary contact point between the Sponsor and the Investigational Site. Responsibilities may include assisting with site selection, pre-trial assessment, subject recruitment and retention planning... ...

Clinical Specialist / Stroke Rater – Chinese Speaking · Location: · Remote · Hours: · Estimated 2–12 hours per month, flexible · Role Overview · The Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality and consist ...

+Clinical Research Associate at ICON plc oversees planning and execution of clinical trials to ensure adherence to timelines, budgets and regulatory guidelines. · +Plan and manage all aspects of clinical trials. · Collaborate with cross-functional teams to establish clinical tria ...

Clinical Specialist / Stroke Rater – Chinese Speaking · Location: Remote · Hours: Estimated 2–12 hours per month, flexible · Role Overview · The Clinical Specialist supports stroke clinical trials by administering standardized assessments and ensuring data quality and consistency ...

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 a ...

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, ensuring adherence to timelines, budgets, · and ...

We are recruiting for a Field Clinical Manager, Interventional Oncology, to be based in one of our major locations: Mainland China, Taiwan, Australia or Singapore. · Acting as a liaison between external healthcare providers (surgeons and interventionalists) and internal teams · S ...

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. · IQVIA is committed to integrity in our hiring process and maintains a zero tolerance poli ...

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 ...