Вакансія Medical Manager в місті Рига
Код вакансії: 61b9ff894b0f430011247d9a
від 3 500 до 4 500 EUR за місяць
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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.


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