Clinical Trial Manager

Clinical Trial Manager

Location [South Korea]

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

The Clinical Team Manager (CTM) is accountable for achieving successful delivery of clinical activities at the project level by meeting internal and external contractually agreed client and regulatory requirements according to time, quality/scope and budget constraints. The CTM leads and directs cross functional teams (Clinical Operations, Regulatory Affairs) and understands/manages client expectations. The CTM proactively identifies, resolves/mitigates and escalates risks and/or issues. Depending on the business unit the descripted ccountabilities may or may not apply.

• Applies knowledge of ICON's policies and procedures
• Manages international clinical teams and multiple trial deliverables
• Demonstrates excellent written and oral communication with internal/external teams and with the customer
• Reads, writes and speak fluent English; and is fluent in host country language
• Demonstrates excellent knowledge of ICH/GCP
• Utilizes clinical knowledge to develop and implement task and trial specific training
• Accurately projects work and resourcing requirements
• Interactions with multi-functional teams and with the sponsor
• Contributes to the preparation and presentation of bid defenses
• Understands associated functions as they relates to Clinical/Trial Management
• Demonstrates working knowledge of Microsoft Office applications, Clinical Trial Management Systems, and Electronic Data Capture platforms

• 3+ years of project management required
• Read, write and speak fluent English; fluent in host country language required.
• Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required.
• 5+ years monitoring experience preferred

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, 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

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