
Job Overview
Location
Remote, China
Job Type
Full-time
Category
Product Management
Date Posted
April 14, 2026
Full Job Description
📋 Description
- • Senior Clinical Research Associate responsible for managing complex clinical trials in Oncology and Rare Disease, ensuring patient safety, data quality, and regulatory compliance across study sites in China.
- • Day-to-day duties include conducting site visits (initiation, routine, close-out), monitoring investigational product handling, verifying informed consent, reviewing source documents, managing site start-up activities, preparing monitoring reports, identifying and escalating risks, and mentoring junior CRAs.
- • Precision Medicine Group integrates clinical trial execution with scientific expertise, laboratory capabilities, and advanced data sciences to accelerate therapy development, with a strong focus on Oncology and Rare Disease.
- • Opportunity to lead complex trials, mentor junior staff, contribute to audit readiness, and gain deep experience in global oncology clinical research within a scientifically driven CRO environment.
Skills & Technologies
About Precision Medicine Group
Precision Medicine Group (PMG) is a leading life sciences consulting firm dedicated to accelerating the development and commercialization of precision medicine. They offer a comprehensive suite of services, including strategy, market access, regulatory affairs, and commercialization support. PMG partners with pharmaceutical, biotechnology, and diagnostic companies to navigate the complex landscape of personalized healthcare. Their expertise spans various therapeutic areas and advanced molecular technologies. By leveraging deep scientific knowledge and market insights, PMG helps clients optimize their drug development pipelines, secure regulatory approvals, and successfully launch innovative therapies. They are committed to advancing patient care through the power of precision medicine, ensuring that the right treatments reach the right patients at the right time.
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