Senior Clinical Trial Manager

Overview

Senior Clinical Trial Manager, China, Beijing/Shanghai/Guangzhou. ICON plc is a world-leading healthcare intelligence and clinical research organization. We are proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

At ICON, it is our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our Own It culture is driven by four values: Accountability & Delivery, Collaboration, Partnership and Integrity. We aim to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touchpoint. If you are driven, join us to work in a dynamic and supportive environment and help shape the industry.

Job functions / responsibilities

(Senior) Clinical Trial Manager

China

Home based or office based

- Act as the Functional Lead from Clinical Operations with responsibility for delivery of all Clinical Operations aspects of clinical studies ensuring consistency with ICON SOPs, study contracts and budgets.
- Build a culture of process improvement with a focus on streamlining processes, adding value to the business and meeting client needs.
- Primary point of contact for Clinical Operations aspects of designated projects.
- Develop successful working relationships with clients. Responsible for planning, scheduling and implementing.
- Contribute to the development and maintenance of cross functional project management plans.
- Lead risk mitigation strategies, associated action plans and issue resolution.
- Lead the Clinical Operations project team, ensure necessary project training is provided to assigned staff, provide direction and support to the study team.
- Collaborate with Business Development to ensure timely completion of change orders.
- Track project deliverables using appropriate tools.

To be successful, you will have

- More than 8 years of professional experience in the clinical research field with at least 2 years of clinical project management experience.
- Experience in managing sites with in depth knowledge of local requirements and regulations across APAC countries including China.
- A bachelor’s degree in a science or medical area. Ideally a master’s degree focusing on clinical research.
- The ability to communicate well, an understanding of compliance as well as the confidence to obtain funding.
- Strong interpersonal skills.
- Good command of written and spoken English.
- Computer literacy.

Benefits and additional information

Benefits of working in ICON include competitive salary packages benchmarked against competitors and annual bonuses tied to performance goals. A range of health-related benefits, competitive retirement plans, and life assurance are provided. The environment supports purpose-driven work and lasting impact.

- Various annual leave entitlements
- Health insurance offerings for you and your family
- Competitive retirement planning offerings
- Global Employee Assistance Programme LifeWorks with 24 hour support
- Life assurance
- Flexible country-specific optional benefits

Visit our careers site to read more about the benefits ICON offers.

ICON is an equal opportunity and inclusive employer. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If you need a reasonable accommodation for any part of the application process or to perform the essential functions of a position, please let us know.

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