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Clinical Project Manager
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Clinical Project Manager
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Are you highly motivated by being able to make a difference to improving patients¡¯ lives?
Are you a high performing executive who energized by challenges and able to energize people around you?
If so, you should continue reading ¡¦
In Novo Nordisk Korea, the position of
Clinical Project Manager
provides you the opportunity to work in
a high performing team to contribute directly towards the business results while creating values for
the Diabetes patients.
About the Department
The Clinical, Medical, Regulatory (CMR) department is one of the key functions that enable the business
strategy through effective execution of functional goals, in the areas of Clinical Research, Medical Affairs,
and Regulatory. The position Clinical Project Manager is to be located at Seoul South Korea, and reports
to the Clinical Development Manager.
The Position
This person should be responsible for multiple clinical trials management in Korea CDC, and ensuring
deliverables are met as per project timelines, within the budget and complying with Protocol, regulatory
requirements, ICH-GCP and NN SOPs.
CDC – Project Management
¤ýConduct overall trial management activities from site selection to post-clinical trial activities, inclusive of
milestones
¤ýBe responsible for coordinating tasks and communication between Regional or Headquarter Trial Managers
and Monitors (CRAs) in order to facilitate progress and global coordination of the clinical trial programme
¤ýBe responsible for escalating issues to local line manager, RTM or HQ TM and seeing to consistency
between the trial sites and CRAs
¤ýProactively drives clinical trial activities forward, and delivers results that have a direct impact on the
successful completion of the clinical programme
¤ýBe responsible for country budget of assigned clinical trial(s)
The Qualifications
Minimum Bachelor¡¯s degree in Pharmacy, life science or nursing
Work Experience
Previous experience in trial management and monitoring in clinical trials in accordance with ICH GCP
at least 7 years, Trial management experience is mandatorily required.
Technical Skills
¤ýExcellent Knowledge of clinical trial methodology and regulation
¤ýUp to date knowledge of the clinical trials environment – ICH GCP, regulatory issues
¤ýProficiency in English
¤ýGood working knowledge of electronic clinical trials systems
¤ýComputer literacy and IT skills
Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for
millions of patients living with diabetes and other chronic diseases. In exchange, we offer the chance to be
part of a truly global workplace, where passion and engagement are met with opportunities for professional
and personal development.
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