Medical Advisor

Review, correct, coordinate, and approve materials for product registration and promotion; review medical instructions for the accuracy of medical information and its compliance with current treatment guidelines and the state register; participate in providing clinical and pharmacological justification for changes made or proposals from other departments, coordinating them with state healthcare authorities if necessary; review submitted materials for the accuracy and ethics of product information; review scientific publications for compliance with the core principles of biomedical research publication; participate in the creation of and assist in the development of marketing materials; provide reliable medical information; prepare clinical and pharmacological justifications for new products; consult employees of the marketing and promotion department; conduct training for marketing and promotion department personnel on therapeutic areas and relevant products; provide medical information support for the Company's websites; consult on post-registration studies (participate in study design development and study documentation); present clinical study results: writing articles, preparing presentations; maintain constructive relationships with leading scientific Key Opinion Leaders; participate in scientific and practical conferences, study scientific literature to enhance professional education; develop medical product strategy together with marketing employees of the marketing and promotion department and healthcare specialists; interact with department line managers; conduct literature analysis, regularly interact with healthcare specialists, structure the information obtained, and prepare science-based proposals for the medical product promotion strategy.

Requirements

• higher medical or biological education and at least 3 years of experience in the same position or in a research organization;
• Required knowledge: Federal Law dated 12.04.2010 N 61-FZ "On the Circulation of Medicines"; Decision of the Eurasian Economic Commission dated 03.11.2016 No. 77 "On Approval of the Rules of Good Manufacturing Practice of the Eurasian Economic Union"; requirements of GOST ISO 13485-2017 Quality management systems. Medical devices; requirements of GOST R ISO 9001 Quality management systems and other legislative acts regulating the area of responsibility; knowledge of medico-biological statistics to the extent necessary for the evaluation and interpretation of scientific and statistical data, including the results of clinical and observational studies; English language proficiency at no lower than intermediate level; ability to work with scientific and medical information, including searching, analyzing, systematizing, and presenting the results of information assessment in therapeutic areas corresponding to the product portfolio promoted by the marketing and promotion department of hospital technologies; skills in writing scientific articles, knowledge of the principles of proper scientific information provision, and organization of scientific and medical events; ability to work in a team and in a multitasking mode; presence of developed communication and presentation skills; proficient oral and written speech.

Higher education — training of highly qualified personnel; Experience: 3 years