Site Engagement Manager, China at Emerald Clinical Trials

Beijing, Beijing, China -

Full Time

Start Date

Immediate

Expiry Date

11 Aug, 26

Salary

0.0

Posted On

13 May, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Site Selection, Relationship Management, Clinical Trial Monitoring, ICH GCP Guidelines, NMPA Regulations, CDE Requirements, Patient Enrollment, Cross-functional Collaboration, Problem Solving, Data Analysis, Chinese Proficiency, English Proficiency

Industry

Biotechnology Research

Description

Who We Are Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world’s top 20pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases, offering Phase I-IV and real-world studies. With over 25 years of experience and a world-renowned focus in renal research, Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality. Global Expertise. Local Insight. Real Impact. Emerald Clinical is where science, speed, and strategy come together to transform healthcare. For over 25 years, we have led the way in clinical research, combining global reach with deep Asia-Pacific expertise and unparalleled local insight to deliver smarter trials and stronger outcomes. Our 800+ employees that span across Asia-Pacific, Europe, and the Americas are embedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward. Key Responsibilities Strategic Site Selection & Partnership Development Support the identification and selection of appropriate investigative sites aligned with study requirements and organizational strategy Establish strategic partnership models with key sites to foster long-term collaboration and mutual value Site Relationship Management Serve as primary point of contact for investigative sites throughout the study lifecycle Build and maintain strong, long-term relationships with PI and site staff Proactively address site inquiries, concerns, and operational challenges Site Performance & Oversight Monitor site enrollment progress and implement corrective actions as needed Conduct accompany site visits (qualification, initiation, monitoring, close-out) as applicable Track site compliance with protocol, GCP, and regulatory requirements Cross-Functional Collaboration Partner with clinical operations, data management, pharmacovigilance, and other functions Align site engagement strategies with overall project goals and timelines Provide site-level insights to support risk management and contingency planning Continuous Improvement Identify opportunities to enhance site engagement processes and tools Share best practices across studies and regions Contribute to site feedback mechanisms to improve sponsor-site partnership Requirements 1. Education - Bachelor's degree or above - Major in Medicine, Pharmacy, Nursing, Life Sciences, or a related field 2. Work Experience - Minimum 4 years of clinical trial-related experience - Experience in site management, monitoring (CRA), clinical operations, or patient enrollment is preferred 3. Travel Requirements - Ability to accept **regular or occasional business travel - Travel is primarily for site visits, investigator meetings, or in-person communication with study sites 4. Professional Knowledge - Familiarity with ICH GCP guidelines and relevant China regulations (NMPA, CDE requirements) - Understanding of the full clinical trial process from start-up to close-out 5. Core Competencies - Strong communication and coordination skills, with the ability to collaborate effectively with investigators, site staff, and internal teams - Problem-solving skills and basic data analysis capability - Ability to work independently while maintaining a team-oriented mindset 6. Language Skills (if applicable for global or multi-regional trials) - Proficient in Chinese (verbal and written) - English reading and writing skills (for handling English protocols or reports) Why Join Us? At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first—both patients and our employees. By joining our team, you’ll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide. Here’s what makes us stand out: • Purpose-Driven Work: You’ll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology. • Global Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial. • Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges. What We Offer We understand that great work happens when people feel valued and supported. That’s why we provide: • Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience. • Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role. • Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role. • Employee Wellbeing: Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events. • Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients. Interested? Apply now and help us achieve our mission to improve the health of millions worldwide. We are an equal-opportunity employer and encourage applications from all qualified candidates.

Responsibilities

The role focuses on strategic site selection and maintaining long-term partnerships with investigative sites to ensure successful clinical trial execution. Responsibilities include monitoring site performance, ensuring regulatory compliance, and collaborating cross-functionally to align engagement strategies with project goals.