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.

This is a rare opportunity to join our friendly global Medical Writing team which sits within ICONs Clinical Research Services group. Our remit is to produce high quality documents supporting clinical studies and regulatory submissions.

• Responsible for writing and reviewing study documents such as Protocol, Synopsis, Informed Consent, Data Collection Documents and Study Report, etc.

• Responsible for developing scientific communication such as abstract, poster, manuscript, etc.

• Responsible for performing quality control for medical writing deliverables

• Responsible for interpreting statistical results and for soliciting statistician input for developing study reports, abstracts, manuscripts, and other documents as required

• Participating in the improvement of the quality assurance system

• Responsible for participating in bid defense presentations representing medical writing activities

• 8+ years of professional experience in Medical Writing at a pharmaceutical, biotechnology, CRO or other health care setting

• Masters’ degree or higher degree in a scientific discipline (medical field or biology)

• Bilingual – Korean and English

• Proven knowledge of ICH/GCP guidelines or other meaningful guidelines or industry standard

• Outstanding written and verbal interpersonal skills

• Good computer literacy

• Ability to work effectively and cooperatively with other team members