SummaryIn line with overall product strategy, the Medical Advisor is responsible for supporting the design, implementation and execution of Medical Affairs plans for assigned Therapy Area, providing scientific information, helping design & organise clinical studies, building educational dialogue with KOLs and regulatory stakeholdersAbout The RoleMajor accountabilities: Ensure medical enquiries are responded to in a high quality, timely manner, and in accordance with applicable standards; establi
SummaryIn line with overall product strategy, the Medical Advisor is responsible for supporting the design, implementation and execution of Medical Affairs plans for assigned Therapy Area, providing scientific information, helping design & organise clinical studies, building educational dialogue with KOLs and regulatory stakeholdersAbout The RoleMajor accountabilities: Ensure medical enquiries are responded to in a high quality, timely manner, and in accordance with applicable standards; establish standard response documents as appropriate, for frequently asked questions.Provide medical/scientific input into the development and execution of clinical trial or clinical research related activities, including initiation and oversight of clinical studies / clinical research within the respective therapeutic area.Support country strategy for Non Interventional Studies/Investigator Initiated Trial activities.Coordinate review and approval of medical materials and locally developed promotional materials; ensure medical materials provided from global or region for stakeholder engagement and events are tailored to local needs, and reviewed/approved per local/BeSure and FUSE guidelines.Ensure medical insights are provided to cross functional groups, including, but not restricted to: Pharmacovigilance, Regulatory affairs, Market Access, QA, Commercial teams, Brand team and others.Responsible for risk identification and assessment, mitigation planning as well as implementation and monitoring of appropriate internal controls within the area of responsibilities.Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)Key Performance IndicatorsWorks within Ethics & Compliance policies -Achievement of annual targets for medical activitiesMinimum RequirementsWork Experience: Collaborating across boundaries.Operations Management and Execution.Project Management.SkillsBuilding Construction.Clinical Practices.Clinical Research.Clinical Trials.Drug Development.Hazard Identification.Health Sciences.Immunology.Intensive Care UnIT (Icu).Internal Control.Internal Medicine.Job Description.Medical Information.Organization Skills.Patient Care.Stakeholder Engagement.Tcp/Ip Protocols.Utilization Management (Um).LanguagesEnglish.Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-cultureJoin our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
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Show lessPosition level
Basic level
Type of employment
Full-time
Job responsibilities
Provider of medical services
Industries
Pharmaceutical production