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The In-house CRA works closely with the Project Manager, Clinical Research Associates (CRAs), and the Clinical Operations team to support the delivery of clinical trials in accordance with local regulations, ICH-GCP guidelines, Novotech/client SOPs, and study protocols. The In-house CRA is responsible for providing operational and administrative support...

The In-house CRA works closely with the Project Manager, Clinical Research Associates (CRAs), and the Clinical Operations team to support the delivery of clinical trials in accordance with local regulations, ICH-GCP guidelines, Novotech/client SOPs, and study protocols. The In-house CRA is responsible for providing operational and administrative support...

Fortrea is seeking an experienced Clinical Research Associate to join our Hong Kong team on-site. You will monitor sites, ensure ICH-GCP compliance, manage source data and regulatory documents, and support trial management activities.The role requires 2+ years of CRA experience, proficiency in English and local language, and a strong understanding of...

ICON plc is seeking a Senior Clinical Research Associate (CRA II) for a client-based role in Hong Kong with flexible work-from-home options. The role involves trial design, monitoring, data review, and collaboration with investigators to ensure patient safety and data integrity. Required: a science/healthcare bachelor's degree, at least 2 years of CRA...

Jiyuan Gene Technology is seeking a Clinical Operations Manager / Senior CRA to lead sponsor-side clinical operations across sites in Hong Kong and international regions. You will handle start-up, site qualification, monitoring, and master file oversight for CG101 and future programs. Experience in Phase I oncology/hematology, CAR-T and related therapies is...

Jiyuan Gene Technology is seeking a Clinical Operations Manager / Senior CRA to lead sponsor-side clinical operations across sites in Hong Kong and international regions. You will handle start-up, site qualification, monitoring, and master file oversight for CG101 and future programs. Experience in Phase I oncology/hematology, CAR-T and related therapies is...

ICON plc is seeking a Senior Clinical Research Associate (CRA II) for a client-based role in Hong Kong with flexible work-from-home options. The role involves trial design, monitoring, data review, and collaboration with investigators to ensure patient safety and data integrity.Required: a science/healthcare bachelor's degree, at least 2 years of CRA...

IQVIA is seeking an on-site Site Monitor in Hong Kong to ensure sites conduct studies according to protocol and regulatory standards. You will perform monitoring visits, train site staff, and manage communications to keep studies on track. The role requires 2+ years of on-site monitoring experience, knowledge of GCP/ICH guidelines, and strong English...

IQVIA is seeking an on-site Site Monitor in Hong Kong to ensure sites conduct studies according to protocol and regulatory standards. You will perform monitoring visits, train site staff, and manage communications to keep studies on track.The role requires 2+ years of on-site monitoring experience, knowledge of GCP/ICH guidelines, and strong English...

OAC Group Limited in Hong Kong seeks a Regulatory Affairs Manager (Pharmaceutical) to lead global regulatory planning and submissions. Reporting to the Head of Regulatory Affairs, you will shape strategy across discovery, preclinical, and clinical programs while aligning filings with development plans.You will drive eCTD submissions for INDs and CTAs,...

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. Summary of...

Fortrea is seeking an experienced Clinical Research Associate to join our Hong Kong team on-site. You will monitor sites, ensure ICH-GCP compliance, manage source data and regulatory documents, and support trial management activities. The role requires 2+ years of CRA experience, proficiency in English and local language, and a strong understanding of...

Primary Responsibilities Non-clinical development strategy and execution For in vivo gene editing pipelines (e.g., liver targeting, ophthalmology, central nervous system, etc.), independently develop and lead high-quality non-clinical pharmacology, pharmacokinetics, and toxicology study strategies in full compliance with NMPA, FDA, and EMA regulatory...

OAC Group Limited in Hong Kong seeks a Regulatory Affairs Manager (Pharmaceutical) to lead global regulatory planning and submissions. Reporting to the Head of Regulatory Affairs, you will shape strategy across discovery, preclinical, and clinical programs while aligning filings with development plans. You will drive eCTD submissions for INDs and CTAs,...

Key Responsibilities l l Clinical Development & Medical Execution: Lead the medical oversight and launch of CSTI-500’s Phase 2 study for Fragile X Syndrome (FXS) in Hong Kong/China, including post‑FDA/NMPA approval activities (CRO medical operations guidance, site selection, investigator initiation meetings). Collaborate with the US team to align...

Key Responsibilitiesll Clinical Development & Medical Execution: Lead the medical oversight and launch of CSTI-500’s Phase 2 study for Fragile X Syndrome (FXS) in Hong Kong/China, including post‑FDA/NMPA approval activities (CRO medical operations guidance, site selection, investigator initiation meetings). Collaborate with the US team to align medical...

Head of Preclinical & Translational Development WearepartneringwithawellestablishedlifesciencegroupasclienttoassisttheirrecruitmentonaHeadofPreclinicalandTranslational...

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. Summary of Responsibilities ...

Primary Responsibilities Non-clinical development strategy and execution For in vivo gene editing pipelines (e.g., liver targeting, ophthalmology, central nervous system, etc.), independently develop and lead high-quality non-clinical pharmacology, pharmacokinetics, and toxicology study strategies in full compliance with NMPA, FDA, and EMA regulatory...

About the roleWe are partnering with a global oncology company headquartered in Switzerland, with commercial operations spanning the US, Europe, and Asia-Pacific. The company has built one of the broadest oncology pipelines in the industry. This is a hands-on regulatory affairs role focused on submission execution and lifecycle management.Key...