Clinical Medical Manager
Novo Nordisk
- 서울시
- 정규직
- 풀타임
- 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
- 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
- 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
- Provide timely guidance and internal training by supporting training creation and delivering training to clinical staff
- 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