Clinical Project Manager

Category:  Clinical Development and Medical

Seoul, Seoul, KR


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 and apply today!

In Novo Nordisk Korea, the position of Clinical Development Center (CDC) 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 report to the Clinical Development Manager. 
The Position
This person should be acountable 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 Novo Nordisk’s SOPs.

The main tasks are the following but are not limited to:

•    Conduct overall trial management activities from site selection to post-clinical trial activities, inclusive of milestones
•    You will be accountable 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
•    You will be accountable for escalating issues to local line manager, RTM or HQ TM and seeing to consistency between the trial sites and CRAs
•    Proactively drives clinical trial activities forward, and delivers results that have a direct impact on the successful completion of the clinical programme
•    You will be in-charge of country budget of assigned clinical trial(s)
•    Minimum Bachelor’s degree in Pharmacy, life science or nursing
•    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.
•    Excellent Knowledge of clinical trial methodology and regulation
•    Up to date knowledge of the clinical trials environment – ICH GCP, regulatory issues, and Good working knowledge of electronic clinical trials systems
•    Proficiency in English and computer literacy and IT skills
Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive change. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 40,000 employees to change the lives for the better for millions of patients living with diabetes and other chronic diseases.
Please click on the link to apply


Until the completion of recruitment
Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.


We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.


At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.