Lead Global Clinical Trials from China and Accelerate Drug Development
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we help accelerate the development of drugs and devices that save lives and improve quality of life. Our success in China is critical to our global mission, and we are seeking an experienced Clinical Trial Manager to lead complex international and domestic studies from a home-based setting.
In this role, you will be the primary driver of clinical trial execution in China, managing all operational aspects from start-up to close-out. You will have the strategic ownership and global support needed to deliver high-quality data on time and within budget, contributing directly to bringing new therapies to patients.
Your Mission: End-to-End Trial Leadership
As the single point of accountability for your studies, you will translate clinical protocols into successful operational reality across China.
Key Responsibilities:
- Strategic Trial Management: Lead the planning, initiation, execution, and close-out of clinical trials, ensuring they are delivered on time, within budget, and to the highest quality standards (GCP/ICH).
- Cross-Functional Leadership: Serve as the central leader for the study team, collaborating seamlessly with global colleagues in data management, regulatory, pharmacovigilance, and project management to align on strategy and resolve issues.
- Site Relationship & Management: Build and maintain strong, collaborative relationships with investigative sites and key opinion leaders (KOLs) across China to ensure optimal site performance and patient recruitment.
- Vendor & Budget Oversight: Manage and oversee local vendors (e.g., Central Labs, CROs) and control the study budget, identifying and mitigating financial risks.
- Proactive Risk Management: Anticipate, identify, and proactively mitigate operational risks to ensure the continuous progress and integrity of the clinical trial.
- Compliance & Quality: Ensure all trial activities adhere to ICON SOPs, local Chinese regulations, and international GCP guidelines.
About You: The Ideal Candidate
You are a proactive and decisive clinical operations professional who thrives on responsibility and delivering results in a complex environment.
Required Qualifications & Experience:
- University degree in medicine, life sciences, or a related field.
- Proven experience as a Clinical Trial Manager (or a Senior CRA ready to step up) with a strong track record of driving studies to successful completion.
- Solid understanding of the Chinese clinical trial landscape, including regulatory requirements and site dynamics.
- Subject matter expertise in one or more therapeutic areas.
- Excellent problem-solving skills and the ability to make critical decisions under pressure.
- Willingness and ability to travel domestically up to 20% for site visits and team meetings.
What Will Make You Stand Out:
- Prior monitoring (CRA) experience is highly valued.
- Experience working on global, multi-center trials.
- Strong leadership presence and exceptional communication skills in both Mandarin and English.
Why Lead Clinical Trials at ICON?
- Global Impact from China: Manage important clinical trials for a world-leading CRO, with your work directly contributing to global drug development pipelines.
- Autonomy & Support: Enjoy the flexibility of a home-based role while being fully supported by a global network of experts and resources.
- Career Acceleration: ICON is committed to nurturing talent. This role offers a clear path for advancement into more senior operational or therapeutic leadership positions.
- Culture of Excellence: Join a diverse and inclusive team that is driven by innovation and a shared mission to shape the future of clinical development.
Comprehensive Benefits Package:
ICON provides a competitive local salary and a benefits package focused on your well-being, including:
- Comprehensive health insurance for you and your family
- Retirement planning programs
- Global Employee Assistance Programme
- Life assurance
- Flexible annual leave
If you are a driven clinical operations leader ready to take ownership of exciting trials, we encourage you to apply. We are committed to responding to every application.
