MEDICAL ADVISOR

Global Responsibility The Medical Advisor (MA) is a member of the Medical department. The MA represents a cross-functional therapeutic and product expert. Her/his role its focus on the development andexecution of the clinical drug development strategy together with the scientific support to drug related regulatory activities.Specific ResponsibilitiesMain AccountabilitiesExecute the clinical strategic global development plans through the execution and management of the of the assigned product.He/she represents the medical department in meetings such as Advisory Board, groups of medical experts, safety committee, regulatory bodies, etc.Perform internal product-related and disease medical training.Create and update the Clinical Development Plan of the assigned product.He/she is responsible for final design and review of study protocols (and itsamendments, if any) and master ICF.He/she is responsible of the review and correct execution of the medical-activities study plans (data review plan, medical management plan, data safety monitoring board plan, statistical analysis plan, medica! data review plan, etc.)Execute the study medical review related to trial.Execute the periodic deviation review meeting.He/she is responsible fer the preparation and release of the Clinical Study ReportSupport the writing and review of the scientific publications to be sent to medical journals and/or congresses.Perform the review for the Module 4 and 5 in the Dossier.Develop the medical response to deficiency letters from the Dossier Expertise and Medical supportTo be recognized as a company expert in the nominated therapeutic areas and provide input into all related product development teams.Provide advice across the company on medical, regulatory and clinical matters and activities relating to assigned product portfolio.Develop and maintain up-to-date knowledge including the competitive environment of the assigned therapy area.Prepares the medical and scientific evidence to communicate the benefits of product portfolio to the market in the pipeline review meeting.Represent the company via presentations to groups of experts and regulatory bodies.Engage Medical Experts and investigators in new clinical trials, identifying partners for future research collaboration, Key Opinion Leaders (KOLs) in Disease Area of research.Mentoring newcomers as requested by the medical department managers.Support medical queries from other departments within the company, as demanded.Pre-Launch activitiesProvide valid and timely interpretations of medical data from medical research in the assigned therapeutic a rea and identify appropriate communication strategy for external and internal stakeholders.Development, attend and represent the medical department at appropriate meetings (advisory board meetings, investigator meetings, KOL meetings, CME, company´s meetings, etc.)AccountabilitiesKPI related to the job.Requirements and personal skillsEducation: Education: Medical Doctor con especialidad (PhD is a big plus?Languages: Fluent Spanish and English.Experience (years/area): At least one year of clinical or research experience.Specific Knowledge: Demonstrable thirst for knowledge with an ability to assimilate information quickly, present clinical data clearly and concisely and discuss the statistical and clinical relevance in line with key messages.Travels: Willingness to travel.Personal skills: Strong organizational, planning and prioritization skills. Costumer oriented personality. Proactive, flexible, decision making and detail oriented. Ability to adapt in a fast-paced environment. Excellent interpersonal skills, working effectively as a team and willing to work in an open and multicultural company. Ability to perform database/literature searches. Clear and effective written/verbal communication skills. Management and leadership skills.