Clinical Medical Manager
Novo Nordisk
- Αθήνα
- Μόνιμη
- Πλήρης Απασχόληση
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:Athens, Athens, GRAre you looking for an opportunity where you can utilize your medical knowledge to communicate scientific data and interact with medical thought leaders? Are you passionate about the world of medical affairs and how it can partner with clinical operations? Are you highly motivated by making a difference to improving patients' lives?If so, you should continue reading and apply today!The role is based in Athens, Greece and reports to the Clinical Medical Manager Lead.The positionAs Clinical Medical Manager, you will be part of the Clinical Medical and Regulatory Department within the affiliate, bridging Medical Affairs and Clinical Operations whilst collaborating closely with relevant stakeholders in IO clinical development, global trial planning and global development. You will help develop New Therapy Areas (with an emphasis on liver, cardiovascular and Alzheimer's disease) and support clinical operations by providing medical/scientific expertise and advice based on interactions with Key Opinion Leaders (KOLs), independent professional associations and patient advocacy associations as necessary. Your area of responsibility will be all areas in Greece, where clinical trials in the above Therapeutic Areas (TA) are conducted.Your Main Responsibilities Will Be:
- To identify and map KOLs, investigators and research centres within the relevant therapy areas, collaborate closely with clinical operations teams during feasibility and allocation process, map patient journey and treatment pathways and facilitate the identification of clinical trial sites, referrals and address educational needs related to New Therapy Areas and clinical trials related to these.
- To collect and discuss relevant early development data with external medical and scientific experts optimizing the feasibility process for clinical trial conduct and provide leadership in the scientific community within New Therapy Areas conducting advisory boards, scientific meetings, engaging with local associations for HCPs on relevant topics.
- To partner with clinical operations to deliver clinical trials 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.
- To provide timely medical guidance and internal training to clinical staff.
- To engage cross-functionally in scientific communication, transferring knowledge between medical and clinical functions. The position requires extensive scientific communication internally as well as externally. Excellent proactive and reactive, attentive communication is a key skill in this role.
- Min. 3 years of medical affairs or clinical research background with solid experience in human healthcare research from within a university or pharmaceutical industry setting
- Previous experience in medical affairs in pharmaceutical company/ies is essential
- Expertise in therapeutic area of relevance, preferably with authorship in peer-reviewed journals
- Experience as clinical trial investigator or sub-investigator is preferred
- Understanding (or willing to learn) of the specificities and nuances of the local healthcare infrastructure
- Understanding of pharmaceutical drug development