Medical Manager

Requirements for candidate:

• M.D, degree, alternatively university degree in pharmacy or life sciences;
• Work experience in medical affairs in pharmaceutical or biotech industry or other stakeholders;
• Not less than 5 years medical / clinical / regulatory / PV experience in pharma industry or any combination of education and experience which would provide necessary skills and qualification;
• Familiarity with industry standards, codes and relevant legislation, including regulatory requirements and standards;
• Knowledge of general medicine and some specialty area, pharmacology and clinical development;
• High level of professionalism, ability and willingness to work effectively with multiple products, projects and partners in cross-functional team setting;
• Excellent communication (verbal and written), presentation, and interpersonal skills;
• Fluent in official national language of the country / countries, and English.;
• Advanced literacy on Microsoft Office applications;
• Readiness for traveling on business purposes

Main responsibilities:

• Supporting company and its Partners' medical activities and providing medical insight to marketing and business development;
• Develop and implement medical strategy plan in the territory as agreed with Partners';
• Providing medical leadership, insight and strategy to company and its Partners' medical and cross-functional teams on local and international level;
• Provide medical strategic recommendation for pipeline and life cycle management programs;
• Developing country medical plans in alignment with global medical strategy;
• Develops relationships with relevant medical groups (e.g. research centres, hospitals, professional associations, patient advocacy groups) in support of company and its Partners' objectives;
• Establishes and enhances strategic partnerships with centres of excellence, key medical and academic institutions and KOLs in areas of scientific interest;
• Planning, designing and managing medical advisory boards and gather insight from regional/national advisory boards; Supporting international advisory boards;
• Provides input to clinical development (clinical study feasibility, support effective study implementation and ongoing management, including disease registries);
• Lead the implementation of medical practices to assess new indications, the treating community, patient pathways, identifying patients for clinical research and to develop a thorough understanding of the disease area;
• Serves as the medical expert and resource within company for the therapeutic area across the territories;
• Provides medical review of field medical tools, internal commercial training material, abstracts and publications, reimbursement dossiers, etc;
• Provide appropriate and timely medical support to commercial team, in line with local standards and regulations;
• Supporting advisory board activities with medical and payer participation and identification of evidence solutions to address data gaps in dossiers and pharmacoeconomic models;
• Defining the country medical resource needs and providing input for medical budget planning, resource allocation and budget management.