* Maintains a level of medical-scientific knowledge in an assigned therapeutic area and/or disease state(s) involving medical and clinical issues related to relevant products * Cooperate With other departments to carry out research projects and the evaluation, particularly in the medical and clinical part of the assessment * Responsible for collection of information regarding existing knowledge gaps, scientific data gaps and clinical care gaps * Provide answers to queries of customers for approved products/indications * Internal and external scientific support, training and education * Provide the Company organization with updated information related to our products and competitors * Develop medical presentations for use in scientific engagements * Responsible for providing inputs from the field into the medical Strategy * Publication support and coordination * Supervise and maintain medical information database * Responsible to check all promotion materials * Other assignment from superior
* Active participation, communication and collaboration with R&D team, Commercial and Marketing department * Creative, Team player, problem settled and work under pressure * Build lasting relationships with clients and prospects * Maintain good working relationships with colleagues, and senior colleagues across the business unit
* Master's degree major in medical science or pharmacy * At least 1 year relevant experience with pharmaceutical company * Fluent and professional English, especially in literature reading, medical writing and oral communication * Deep knowledge of the therapeutic area, strength in research and interpretation of medical data * Clinical trial protocol knowledge * Strategic thinking and business insights * Strong organizational and problem solving skills * Demonstrated ability to deliver results to the appropriate quality and timeline metrics * Good team leadership skills, good judgment and effective presentation skills * Establish and maintain effective working relationships with clients * Familiar with applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines * Software and computer skills, including MS Office applications