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Senior Clinical Trial Manager

Employer
ICON Plc
Location
China, Homeworking
Salary
Competitive
Start date
10 Jun 2024
Closing date
21 Jun 2024

Job Details

At ICON, it’s 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 key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That’s our vision. We’re driven by it. And we need talented people who share it.
If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

(Senior) Clinical Trial Manager

China

Home based or Office based

Job functions/responsibilities

As (Senior) Clinical Trial Manager, you will 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.

•You would be expected to build a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs.

•Primary point of contact for Clinical Operations aspects of designated projects.

•Responsible for developing successful working relationships with clients Responsible for planning, scheduling and implementing.

•Contribute to the development and maintenance of cross functional project management plans.

•Responsible for risk mitigation strategies, associated action plan and issue resolution.

•Responsible for leading the Clinical Operations project team, including ensuring all 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 filed with at least 2 years of clinical project management experience;

•Experience in managing sites with in depth knowledge in local requirements and regulations across APAC countries including China;

•A bachelor’s degree in a science or medical area. Ideally you’ll have a master’s degree that focuses 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 of Working in ICON:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you’ll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. 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, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

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