Senior PM

Senior PM 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 registration to post-marketing. Our therapeutic expertise spans renal , cardiometabolic , and oncology —areas where we make a significant impact on improving global health. At the heart of our success is our ability to combine global reach with local knowledge. Our on-the-ground teams work closely with local communities, building trust and ensuring diverse, representative patient recruitment. By prioritizing people, we deliver better engagement, more accurate data, and faster results—bringing therapies to patients in need. 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. About the Role • be responsible for owning and achieving interim and final contractual deliverables for assigned projects/programs, according to the time, quality/scope and cost constraints. including adherence to all relevant regulations including GCP, ICH and Regulatory requirements, as well as applicable SOPs and policies. • be responsible for managing assigned as study budget, timelines, and risk mitigation • Acts as primary liaison with client: -Acts as lead contact for regional and or/project matters. -Understands/manages/satisfies client contractual, organizational and relationship needs/expectations. -Provides regular reporting on project metrics, status of deliverables and risks/issues with the associated management plan to client. -Chairs and leads client meetings. • Leads and directs cross-functional team leaders and third parties/vendors: • Be responsible for project contractual deliverables and cost: • Be responsible for BDM supporting • process input from key stakeholders, communicating to other function, as appropriate. • support the development and application of standardized operational study processes, methodologies, appropriate quality and performance metrics and tools to systematize continuous process improvement and impart best practices across clinical operations to maximize its effectiveness. Your Responsibilities • in-depth knowledge of clinical drug development processes and experience applying GCP, ICH and FDA requirements. • Excellent written and verbal communication. • The ability to generate concise summaries for different audiences, professional correspondence, presentations, reports, and training materials. • Literacy in word processing, spreadsheets, and databases applications (e.g., MS Word and Excel). • Skilled at developing project timelines and milestones and working with team to ensure milestones are met; adjusts appropriately when needed and communicates risks when necessary. • strong communication skills to be able to discuss with the Sponsor and Investigators. • Ability to identify and articulate risks and benefits of plan. • solid knowledge of clinical research study protocol and processes; ability to incorporate and adhere to GCP and regulatory standards. Ability to develop study processes in support of a clinical study design. About You • BS degree and above in related medicine preferred. • Excellent written and verbal communication in English. •With MRCT experience or experience in Global CRO or Global Pharma, undertake at least one complete project as a PM. •With experience in Oncology or renal disease projects are preferred • 6 or more years related experience in clinical study execution. 3 years related experience in project management. • experience leading a study or significant participation on study team through major milestones. • experience in vendor management • system experience: (i.e., CTMS, eDC, eTMF etc.). • experience in BDM or other project delivery presentation. 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. Department Project Management Locations CHINA - WUXI - Beijing, CHINA - WUXI - SHANGHAI, China - Guangzhou, CHINA - WUXI - Wuhan Remote status Hybrid