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1 VAGA DE Médico EM Rio de Janeiro / RJ
Função/cargo da vaga:
Médico
Empresa:
Nome da empresa disponível para cadastrados.
Salário:
A combinar
Cidade/Estado:
Rio de Janeiro / RJ
Tipo de Vaga:
Home Office
Regime de contrato:
Efetivo/CLT
Descrição da vaga:
Invitae is a leading genomic information company with an expanding international reach and a mission to drive better access to genomic healthcare within mainstream medical practice. Invitae’s global medical affairs team has open positions for experienced individuals to support the company’s medical affairs activities in various global geographic regions. This medical affairs director - International role is responsible for providing medical support to achieve the objectives and strategies of the invitae’s international sales, business development, and marketing teams. By providing the necessary professional medical presence at client interactions, at regional scientific conferences, and in discussions with key opinion leaders, healthcare institutions, and potential biotechnology partners, the ma director ensures that invitae’s products and services are appropriately presented to and contextualized for clients and partners. This role is also involved in performing due diligence on scientific and business opportunities, and in securing partnerships that enhance invitae’s mission of enabling access to genetic information for a broader population. Invitae routinely collaborates with academic, commercial, and other types of partners, including clinical centers of excellence, biopharmaceutical companies, healthcare businesses, and patient advocacy groups. This role is also responsible for researching and responding to rfps, identifying and engaging key opinion leaders, and bridging relationships with professional and conference committees. The medical affairs director role requires a deep understanding of hereditary disease, germline and somatic genetics, genetic testing methodologies, interpretation of sequence and copy number variation, and the current clinical trends, local standards of clinical care, and client expectations of services related to genetic testing. What you will do: identifying and developing relationships with key opinion leaders and with professional practice committees across different clinical areas supporting local laboratories and clinicians to help them use invitae products to generate data in their labs (local evidence generation for regulated product launches) collaborating with local laboratories and clinicians to generate data and publications to promote wider clinical use. This includes evidence generation to support broader use of invitae’s products interacting with biopharmaceutical partners to generate data prior to product launch, to provide ongoing support, and help navigate regulatory issues providing direct medical support to invitae’s international sales and marketing teams with strategic planning of yearly and long-Term goals identifying and securing scientific collaborations. Responding to incoming international collaboration requests and client inquiries in coordination with medical affairs program managers educating clients on invitaes test menu in coordination with the international sales field team host and help organize speakers for professional education at local events providing remote and on-Site educational consultations on invitae’s genetic testing products/services engage with local committees, societies and associations to drive discussions surrounding clinical utilization, product requirements, and establishment of local guidelines delivering academic presentations at conferences and providing support at invitae’s sponsored sessions and booths presenting at meetings with healthcare systems, third party payors, academic institutions, and others establishing relationships with key opinion leaders supporting sales training for the international commercial team guiding feedback on invitae’s products and services to the international sales team and the global medical affairs team preparing strong rfps in response to opportunities in collaboration with medical affairs liaisons who you are: M.D. Or ph.D. Degree with genetics training expertise in clinical molecular genetics applicable to both germline and somatic genetics and across clinical areas, including oncology. Minimum of 3 years of experience director experience in medical affairs or a commercial clinical genetics laboratory setting visible stature in the local medical genetics community through participation in academic and professional societies. Requisitos: conhecimentos: access
Cód. 6733894
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