
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.