Senior Clinical Research Associate – Global Site Monitoring

Essential Functions Manage assigned sites and perform Subject Level Data Review independently, if required perform with both responsibilities as dual role.; Perform remote monitoring visits for assigned sites as assigned.; Perform Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy (inclusion &...

A leading clinical research organization in Hong Kong is seeking professionals to manage clinical trial sites and perform data reviews. The ideal candidate should hold a Bachelor’s degree in clinical or life sciences and have a minimum of 2 years’ experience. This role requires strong organizational, communication, and problem-solving skills to ensure...

A global clinical research provider in Hong Kong is seeking a qualified individual to manage staff and ensure high-quality performance in clinical research projects. The role requires a Bachelor’s Degree in a scientific discipline or health care, relevant clinical trial experience, and strong leadership skills. Proficiency in Microsoft Office tools and...

What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution. Collaborating with cross-functional teams to ensure timely and...

Medical Advisor/Associate Director (Endocrinology/Neurology) Primarily serves as Regional Medical Advisor on assigned projects. Serves as Scientific Advisor and provides guidance to Project Leaders on the medical and scientific aspects of assigned projects. Provides medical support to investigative sites and project staff for protocol-related issues...

A leading healthcare intelligence organization in Hong Kong seeks a Senior Statistical Programmer to analyze clinical trial data and develop statistical programs in SAS. Successful candidates will collaborate with biostatisticians, conduct quality control on outputs, and prepare statistical reports. Ideal applicants hold a degree in Statistics or related...

Role: Clinical Specialist/Clinical Trial Rater As a Clinical Specialist Consultant, you will play a crucial role in ensuring the reliability and standardization of assessments in clinical trials. Your responsibilities will include: Reviewing scales administered by raters to ensure standardized assessments. Conducting patient assessment and administering...

A leading global clinical research provider in Hong Kong seeks a Clinical Specialist/Clinical Trial Rater to ensure reliable assessments in clinical trials. The role involves reviewing scales, conducting patient evaluations, guiding raters, and managing documentation. Required qualifications include a Master’s degree in a relevant field, at least 3 years...

Senior Statistical Programmer 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 development We are currently seeking a Senior Statistical Programmer I to join...

A leading global clinical research provider in Hong Kong is seeking a Medical Advisor/Associate Director to oversee projects in the endocrinology and neurology fields. The role involves providing critical medical support, reviewing relevant medical documentation, and attending client meetings. The ideal candidate has expertise in the required therapeutic...