Clinical Research Associate – Site Monitoring Lead

A global clinical research organization in Hong Kong is seeking a Clinical Research Associate to oversee site management for clinical trials. The successful candidate will be responsible for ensuring compliance with regulatory guidelines, conducting monitoring visits, and safeguarding data integrity. Candidates should have a B.A./B.S. in Life Sciences or...

A clinical research organization in Hong Kong is seeking an Associate for project management and site management of clinical studies. Responsibilities include site selection, training site staff, ensuring compliance with regulations, and managing budgets. Ideal candidates should have a Bachelor's degree in a related field and at least one year of experience...

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...

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 leading global clinical research provider in Hong Kong is looking for a Senior Clinical Research Associate to manage site monitoring and ensure adherence to study protocols and regulations. Ideal candidates should have at least one year of on-site monitoring experience and a Bachelor's degree in a scientific discipline or healthcare. Strong communication...

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...

(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...

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...