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/P3 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)
Qualifications
Experience: At least 3 years in pharmaceutical companies, including medical department or clinical practice roles.
Clinical Design and Research: Expertise in creating clinical designs and analyzing English papers. Proactively updates and shares information.
Innovative Environment Creation: Fosters innovation and new product launches while collaborating with related departments.
Ethical Communication: Communicates clearly and flexibly with internal and external customers, based on ethical awareness.
Team Collaboration and Independence: Respects team diversity, collaborates effectively, and works independently in various situations.
