Job Overview
Location
Remote, China
Job Type
Full-time
Category
HR & Recruiting
Date Posted
April 14, 2026
Full Job Description
đź“‹ Description
- • As a Drug Safety Lead at Precision Medicine Group, you will play a critical role in ensuring patient safety and regulatory compliance in clinical trials, directly contributing to the advancement of life-changing therapies in oncology and rare diseases.
- • Your day-to-day responsibilities will include leading safety budget reviews, developing safety management plans, overseeing serious adverse event (SAE) case management from intake to regulatory reporting, interfacing with sponsors and vendors on safety collection tools, preparing and reviewing safety documentation, mentoring Safety Specialists, participating in audits and CAPA processes, and serving as a subject matter expert for pharmacovigilance activities.
- • You will join a specialized team at Precision for Medicine, a forward-thinking CRO that integrates clinical trial execution with deep scientific expertise, laboratory capabilities, and advanced data sciences to accelerate drug development, with a strong focus on oncology and rare disease therapeutics.
- • In this role, you will deepen your expertise in global pharmacovigilance regulations, lead cross-functional safety initiatives, mentor junior staff, influence safety strategy and process improvements, and gain visibility into high-impact clinical programs supporting breakthrough cancer therapies.
🎯 Requirements
- • BA/BS degree
- • 10+ years of clinical safety experience
- • 5+ years of Pharmacovigilance (PV) experience
- • Hands-on experience with global safety databases, SAE case processing, and safety report generation
- • Working knowledge of MedDRA, WHODrug, FDA safety regulations, ICH guidelines, and global pharmacovigilance requirements
- • Excellent communication and analytical skills (written and oral), with the ability to convey complex clinical issues clearly and scientifically
🏖️ Benefits
- • Opportunity to work on impactful oncology and rare disease clinical trials that advance life-changing therapies
- • Remote work flexibility based in China
- • Professional growth through mentorship, leadership, and involvement in cross-functional initiatives and audit readiness
- • Supportive culture that values employee contributions, encourages idea-sharing, and fosters positive change
- • Employment with an Equal Opportunity Employer committed to diversity, inclusion, and fair hiring practices
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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