Senior Clinical Research Associate

Clinical Research Associate II/ Senior Clinical Research Associate 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...

Clinical Research Associate II/ Senior Clinical Research Associate Join ICON Strategic Solutions as a Clinical Research Associate II/ Senior Clinical Research Associate. CRA II/ Senior CRA - office-based in Hong Kong. Join us and advance your career with an industry leading CRO. ICON plc is a world-leading healthcare intelligence and clinical research...

CRA II/ Senior CRA - office-based in Hong Kong. Join us and advance your career with an industry leading CRO. 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 clinical...

A clinical research center in Hong Kong is looking for a candidate to support daily operations and administrative work related to clinical trials. Responsibilities include data entry, processing study specimens, and participating in outreach activities for recruitment. An Associate Degree in Science or Pharmacy is required, along with strong English and...

A leading clinical research organization is seeking a Senior Clinical Research Associate in Hong Kong. In this role, you will oversee clinical trial activities ensuring compliance with protocols and regulatory standards. The ideal candidate should have an advanced degree in life sciences and extensive CRA experience. ICON offers competitive salary and a...

Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close‑out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH‑GCP),...

A clinical research organization in Hong Kong is seeking a Clinical Research Associate to manage clinical studies and ensure compliance with ICH GCP Guidelines. The role requires 1+ years of Clinical Monitoring experience and fluency in both Cantonese/Mandarin and English. Responsibilities include site monitoring, data integrity verification, and preparing...

(Senior) Clinical Research Associate (CRA) 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 monitoring visits (selection, initiation,...

International Business Unit Functional Support Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good...

Support clinical center's daily operation Support administrative work to support clinical trials conduct - including but not limited to documents preparation and archival, data entry Process study specimens Have opportunities to coordinate minor projects Ensure high quality of work meeting Good Clinical Practice (GCP) and other applicable regulatory...