- Acting in the dissemination, clarification and education of scientific data and study protocols proactively and reactively according to local and global regulations for health professionals.- Identification and segmentation of opinion leaders.- Planning and execution of strategies directed according to the medical profile.- Marketing support in annual strategic planning.- Performance in the generation of competitive intelligence data through scientific and market information.- Classes directed to physicians, pharmacists and responsible for health institutions and health care providers.- Support the access team with classes for administrators and technical clarification related to pathologies, medications, ANS Rol and DUT in force.- Responsible for training the sales force and other internal areas of Bayer with regards to ophthalmology topics.- Participation in national and international congresses- Coordinator of scientific education activities: "Young Retina Meeting 2018/2019"- Support the clinical research team in the prospection of study centers and assistance in operational and strategic feasibility visits.- Responsible for reporting cases of adverse events to the pharmacovigilance group.

- Promptly and accurately interpret and enter serious and non-serious adverse events into the global database for distribution.- Perform assessment of cases regarding the global listedness.- Create comprehensive narratives procured from relevant, related information from various source documents.- Request all pertinent follow up information from local affiliate for the completion of case reports within specific timelines as prescribed by global regulations and SOPs.- Accurate coding of incoming serious and non-serious adverse events using MedDRA terminology.- Verify, as prescribed by regulatory guidelines, that trade names are correctly translated into INN (Internation Non-proprietary Name)- Overall representation of the case and defined data entry fields are checked and validated against the source documents and/or the data provided by the PVCH. If applicable, cases are corrected and further actions initiated according to standard case processing practice.

- Plans and coordinates the initiation of research study protocol, and the establishment of operating policies and procedures. - Plans, implements, and maintains data collection and analysis systems in support of research protocol; may coordinate the collection and analysis of research data. - Ensures the smooth and efficient day-to-day operation of research and data collection activities- Recruits, instructs, and coordinates research subjects as appropriate to specific study objectives and work scope. - Coordinates the day-to-day activities of any technical support staff specifically engaged in the carrying out of clinical protocol.- International meetings participation (discussion of study protocol).