Senior Clinical Research Associate

(Senior) Clinical Research Associate (CRA) Add expected salary to your profile for insights 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...

A leading global clinical research provider is seeking a Senior Clinical Research Associate in Hong Kong. You will be responsible for monitoring clinical sites, ensuring compliance with regulatory guidelines, and managing study progress. Ideal candidates should have at least 1 year of on-site monitoring experience and a Bachelor’s degree in a scientific...

Clinical Trials Assistant (CTA) (Evergreen) Posted 6 days ago. Be among the first 25 applicants. Job Overview 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. Essential Functions Assist Clinical Research Associates...

A leading global clinical research provider is seeking a Clinical Trials Assistant (CTA) to support the Clinical Research Associates and Regulatory teams in maintaining trial documentation and ensuring compliance. Responsibilities include managing clinical documents, assisting with study files, and preparing clinical trial supplies. Ideal candidates should...

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, monitoring and close-out visits) in accordance with...

A global clinical research organization is seeking a Clinical Research Associate in Hong Kong to perform monitoring and site management for clinical studies. You will ensure compliance with protocols and regulatory requirements. The ideal candidate has a Bachelor's Degree in a relevant field, at least 1 year of on-site monitoring experience, and strong...

Job Overview 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. Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...

A leading global provider of clinical research services, this company is seeking a Site Activation Specialist to manage site activation and regulatory activities. The successful candidate will handle documentation and serve as a key contact for investigative sites, requiring a Bachelor's in Life Sciences and related experience. This full-time position offers...

A leading clinical research organization in Hong Kong seeks an Administrative Support professional to assist Clinical Research Associates and Regulatory teams in managing trial documentation and supplies. The ideal candidate has a High School Diploma and 3 years of administrative experience. Key skills include proficiency in Microsoft Office and a good...

Postdoctoral Fellow/Research Associate/Research Assistant (Immuno-Oncology Research) The long-term objective of the Centre for Oncology and Immunology is to employ novel functional screens, animal and cell models including organoids, immuno-oncology approach, as well as advanced genomic and proteomic techniques down to single cell resolution to identify...