Under moderate supervision, the Regulatory and Start Up Specialist executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. Prepares and manages
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as an Assistant Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750
Descrição da empresa A QIMA Life Sciences é uma divisão de rápido crescimento do Grupo QIMA, dedicada a fornecer serviços completos para a indústria de ciências da vida – desde P&D até o lançamento no mercado.
Job Overview: Senior Site Navigators play a critical role in the comprehensive coordination of site-level activities throughout the start-up phase of a clinical study and potentially through closeout activities as required. Serving as the single point
Senior Site Partner ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our
Crinetics is a pharmaceutical company headquartered in San Diego, California, with a growing presence in Latin America, including an office in Brazil. We are developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We
# Sr. Site Activation Specialist in BrazilApplylocations: São Paulo, Braziltime type: Full timeposted on: Posted Yesterdayjob requisition id: R Under moderate supervision, the Sr . Site Activation Specialist executes the feasibility, site identification regulatory, start-up, and
# Site Activation Specialist in BrazilApplylocations: São Paulo, Braziltime type: Full timeposted on: Posted Yesterdayjob requisition id: R Internal Job DescriptionUnder moderate supervision, the Site Activation Specialist executes the feasibility, site identification regulatory, start-up, and maintenance
SOLTI is an academic research group that performs clinical trials of excellence in oncology. Currently, SOLTI is comprised of over 550 renowned research professionals distributed over a broad network of more than 100 leading hospitals in
REQUISITOS TÉCNICOS OBRIGATÓRIOS: Curso Técnico de Enfermagem concluído; Registro Profissional no Conselho ativo COREN MG; Possuir habilidade e conhecimento para a execução de todos os procedimentos de enfermagem exclusivos do técnico de enfermagem; Conhecimento do Código
Descrição : A área de Comercial de Crédito e Serviços é responsável pelo fomento comercial, desenvolvimento de produtos, ações comerciais e capacitação das cooperativas centrais e singulares do Sicoob para os produtos de crédito, sejam eles
Descrição : A área de Comercial de Crédito e Serviços é responsável pelo fomento comercial, desenvolvimento de produtos, ações comerciais e capacitação das cooperativas centrais e singulares do Sicoob para os produtos de crédito, sejam eles
Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.
The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions. This role will be responsible