Remote CRA: Clinical Trials

A global Contract Research Organization is seeking a highly organized Project Specialist to join their Early Phase Project Management team in Hong Kong. The role involves supporting project managers in delivering global clinical trials, maintaining project documentation, and coordinating meetings. Candidates should possess a relevant bachelor's degree and...

A global clinical research organization is seeking a Clinical Research Associate II in Hong Kong. In this role, you will design and analyze clinical trials, ensuring patient safety and protocol compliance, while collaborating with investigators. The ideal candidate should have a Bachelor's in a scientific or healthcare field and at least 2 years of relevant...

A global healthcare solutions provider is looking for a Clinical Research Associate to join their team in Hong Kong. The role entails conducting and monitoring clinical trials, ensuring compliance with regulations, and collaborating with site staff. Candidates should have a Bachelor's degree in a related field and at least 2 years of experience. This...

Medpace Clinical Trial Manager – Infectious Disease Medpace is a scientifically led organization offering full-service solutions for our clients, giving the Medpace project teams the empowerment to truly lead and execute clinical trials. The Clinical Trial Manager position is the lead role for multiservice global/regional clinical trials. The CTM interacts...

A clinical-stage biotechnology company is seeking an Associate Director to Director in Biostatistics. This role involves providing statistical leadership across clinical trials and programs, ensuring scientific integrity, and collaborating across functions. Candidates should have a Ph.D. in Biostatistics and experience in the pharmaceutical industry. The...

A leading clinical research organization in Hong Kong is seeking a Clinical Site Associate (In-House CRA) to support clinical trial operations. This hybrid office role will involve managing site communications, ensuring compliance, and supporting site readiness activities. Ideal candidates will have a Bachelor's degree in a relevant field and possess strong...

At Emerald Clinical Trials , we are a global, full-service Contract Research Organization (CRO) with a rich heritage in the Asia‑Pacific region. We are dedicated to advancing clinical research through scientific expertise and operational excellence, supporting biopharmaceutical, medical device, and diagnostic customers across all trial phases, from...

A leading global clinical research firm is seeking a Clinical Specialist to support stroke clinical trials by administering assessments and ensuring data quality. You will work flexibly, participating in interactions with trial participants, maintaining protocol compliance, and contributing to the consistency of assessments. A Master’s degree in a relevant...

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...

A leading clinical research organization is seeking a Clinical Site Associate in Hong Kong. This role involves managing site communications, supporting trial operations, and ensuring site compliance with protocols. Candidates should possess a Bachelor’s degree in a relevant field and have previous experience in clinical research. Ideal applicants will...