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Clinical Medical Manager

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Onsite

Clinical Medical Manager

Novo Nordisk

Clinical Medical Manager

2 months ago

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Important information


Contract type:

Permanent

Location:

Incheon, South Korea

Work mode:

Onsite

Published on:

30 August 2026

What they need


Are you passionate about clinical trials and making a difference in the field of healthcare? Do you have expertise in New Therapy Areas such as Cardiovascular disease, Chronic Kidney Disease, Liver Disease, inflammation, and emerging therapy areas? We are looking for a Clinical Medical Manager to join our team at Novo Nordisk. Apply now for a life-changing career!

About The Department The Clinical Medical Management Unit at Novo Nordisk is a dynamic and collaborative team devoted to advancing healthcare through clinical research and development. We work closely with key opinion leaders, investigators, and research centers to drive innovation and improve patient outcomes. Our department is fast-paced and offers opportunities for growth and professional development.

The position As a Clinical Medical Manager (CMM), you will facilitate clinical trials in multiple therapy areas including diabetes, obesity, cardiovascular disease, liver disease, kidney disease and emerging therapy areas by providing medical/scientific executions impacts based on insights from investigators. Demonstrate independence, innovation, and initiative in prioritizing and performing scientific tasks. This role may require some international travel for site visits, congresses, and company events.

Your Key Tasks Are

  • Contribute to successful clinical trials by collaborating with clinical operations to drive scientific execution activities and leverage investigator’s scientific expertise through scientific activities and site selection and initiation visits, performing ad hoc visits, engaging key investigators to be the industry leader in trial execution and upskill investigators in medical treatment with investigational medicinal product.
  • Build trial strategy for scientific execution and drive industry leading scientific activities to contribute to scientific retention and recruitment (SRR) activities locally and build strong scientific partnership with investigators, site staff, and relevant stakeholders to ensure smooth study conduct and timely trial execution based on insights.
  • Provide timely medical guidance and training to clinical staff by supporting training creation and delivery.
  • Identify and map potential investigator candidates, investigators, and research centers in relevant therapy areas in collaboration with clinical operations teams. Engage with investigators to collect valuable medical insights to build relevant trial strategy and execute cross-functional activities within the local affiliate/Clinical Development Center (CDC) and cross-country teams.
  • Collect early scientific insights and guidance by discussing relevant development data with external medical and scientific experts, engaging with clinical experts for trial execution excellence, and ensuring internal and external stakeholders are trained on the trial's scientific background. Act as an expert in relevant TAs and lead trial execution relevant scientific activities through medical initiatives e.g. advisory boards, scientific meetings, and engagement with investigators. Support ad hoc requests with timely scientific and medical responses for investigators, site staff, clinical operations staff, and other relevant stakeholders.

Qualifications

  • MD or Ph.D, PharmD, Pharmacist in healthcare industry with strong clinical and medical, research background is essential.
  • Require as minimum 5 years or more of Medical affairs experience in pharma nidustry, solid expertise in relevant therapeutic areas, and experience in human healthcare research, preferably with peer-reviewed journal authorship. Clinical/pharmaceutical industry experience would be added advantage.
  • Understanding of the specificities and nuances of the local healthcare infrastructure and pharmaceutical drug development.
  • Extensive scientific communication skills for internal and external stakeholders, excellent and proactive communication skills, and strong presentation abilities.
  • This position is only open to local language speaking Korean applicants, with native language fluency in Korean.

Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. 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. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.

Contact Kindly upload your CV to our online career page (click on Apply and follow the instructions).

Internal candidates are requested to inform their line manager when applying.

Deadline 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're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

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