Clinical Research Associate: Onsite Study

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...

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),...

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...

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...

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...

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...

(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,...

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interview. If you're pre-selected, our recruiter will keep in touch and let you know when the role officially opens, so we can reconfirm your interest before moving forward with an offer. Responsibilities Site management...

Add expected salary to your profile for insights Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interview. If you're pre-selected, our recruiter will keep in touch and let you know when the role officially opens, so we can reconfirm your interest before moving...

Responsibilities Monitor clinical research studies to ensure compliance with widely accepted clinical practices e.g. ICH/GCP; Serve as primary Sponsor contact for project-specific issues and study deliverables; Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates;...