Clinical Medical Manager

Novo Nordisk

  • 서울시
  • 정규직
  • 풀타임
  • 2개월 전
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Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading...Category×Select how often (in days) to receive an alert:×Select how often (in days) to receive an alert:Clinical Medical ManagerCategory: Medical AffairsLocation:Seoul, Seoul, KRAre you looking for an opportunity where you can utilize your medical knowledge to communicate scientific data and to interact with medical thought leaders? Are you passionate about the world of clinical trials? Are you highly motivated by being able to make a difference to improving patients' lives?If so, you should continue reading and apply today!The position's key responsibilitiesThis position is expected to facilitate execution of clinical trials related to New Therapy Areas (including Cardiovascular disease, Chronic Kidney Disease, Liver Disease, inflammation, Alzheimer's disease and emerging therapy areas) by providing medical/scientific expertise and advice based on interactions with KOLs, independent professional associations and patient advocacy associations as necessary.1: Identify KOLs, investigators and research centres
  • Identify and map KOLs, investigators and research centres within the relevant therapy areas
  • Collaborate closely with clinical operations teams in CDC, region, IO-So and HQ during feasibility and allocation process
  • Identify and engage with relevant patient advocacy groups and investigate areas of mutual interest and potential collaboration
  • Collect medical insights that may be of value to Novo Nordisk and cascade these as relevant to region as well as cross-functionally within local affiliate/CDC
2: Collect early scientific insights and guidance
  • Discuss relevant early development data with external medical and scientific experts optimizing the feasibility process for the clinical trial conduct
  • Identify and regularly engage with clinical experts in relevant TAs to obtain guidance relevant to clinical trial execution
  • Ensure site staff at main site and referral centres are properly trained on the scientific background of the trial and act as subject matter expert within relevant TAs
  • Provide leadership in the scientific community within New Therapy Areas conducting advisory boards, scientific meetings, engaging with local associations for HCPs on relevant topics
  • Support ad hoc requests by providing scientific and medical responses to requests from KOLs, HCPs, site staff, clinical operations staff and other stakeholders in a timely manner
3: Contribute to Clinical activities
  • Contribute to delivering successful clinical trials (phase I-IV) in collaboration with clinical operations including driving scientific discussions at site selection and initiation visits, performing ad hoc visits, supporting attendance at investigator meetings, ensuring KOL inclusion in clinical trials, and engaging key investigators to communicate trial results
  • Contribute to scientific retention and recruitment (SRR) activities at local level
  • Ensure continuous dialogue with investigators, site staff and other relevant stakeholders to ensure smooth study conduct and to collect timely and relevant insights throughout the duration of the study
  • Support process on Investigator Sponsored studies by contributing to evaluation of proposals and ensuring follow-up after approval in close collaboration with local Medical Affairs team
4: Deliver Medical guidance
  • Provide timely guidance and internal training by supporting training creation and delivering training to clinical staff
Qualifications
  • MD or PhD, PharmD, Pharmacist in healthcare industry with strong clinical and medical, research background
  • At least 5 years of clinical or pharmaceutical industry experience, especially solid experience with healthcare research either from university or pharmaceutical industry
  • Expert in therapeutic area of relevance, preferably with authorship in peer-reviewed journals
  • Understanding the specificities and nuances of the local healthcare infrastructure and pharmaceutical drug development
  • Experience as clinical trial investigator or sub-investigator is preferred
Working at Novo NordiskAt 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.ContactUpload your CV to our online career page (click on Apply and follow the instructions).DeadlineUntil the completion of recruitmentApplications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.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.

Novo Nordisk

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