Job Type






Clinical Trial Manager South Korea


ICON - APAC South Korea Korea, South

2 months ago

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.

Clinical Trial Manager - Late Phase/PMS

Home based, Korea

The Clinical Trial Manager is responsible for the delivery of all clinical aspects of the study.
The CTM oversees the clinical portion of the budget, develops monitoring plans & tools, trains CRAs, drives enrolment and study start-up activities, reviews trip reports... implements corrective and preventative action plans, liaises with the Sponsor, vendors & cross-functional teams, identifies & mitigates risks that may impact clinical delivery, and provides reporting & metrics on all clinical activities.
The CTM will also participate in Sponsor, Investigator and bid defense meetings.
• Primary point of contact for Clinical Operations aspects of designated projects and responsible for developing successful working relationships with clients
• Responsible for planning, scheduling and implementing the Clinical Operations aspects of projects
• Contribute to the development and maintenance of cross functional project management plans
• Responsible for risk mitigation strategies, associated action plans and issue resolution
• Responsible for managing the Clinical Operations project team, including ensuring all necessary project training is provided to assigned staff
• Provide direction and support to the Clinical Operations study team
• Manage Clinical Operations aspects of projects in accordance with the contract including communicate any changes in Clinical Operations scope to the Project Manager and collaborate with Business Development to ensure timely completion of change orders
• Track Clinical Operations project deliverables using appropriate tools
• Effectively monitor and report on progress of the Clinical Operations aspects of projects to all stakeholders
• Implement QC activities as necessary and monitor required quality metrics
• Participate in business development activities, as appropriate including bid defense and proposal activities
• Responsible for managing the Clinical Operations project team, including ensuring all necessary project training is provided to assigned staff

You will need:
• 4 year degree or equivalent combination of education & experience

• 7+ years of experience in the clinical trial including minimum 1+ year of Lead CRA/Clinical Trial Manager

• Late phase and/or PMS study experience is required
• Demonstrated ability to drive the clinical deliverables of a study
• Subject matter expertise in the designated therapeutic area
• Prior monitoring experience is preferred
• Fluent in local language as well as English - both written & verbal

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.
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
South Korea

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