
1001 - 5000 funcionários
Fundada em 1958
🏥 Saúde
💼 Consultoria
📦 Logística
Healthcare • Consulting • Logistics
O RTI International é um instituto de pesquisa independente sem fins lucrativos dedicado a melhorar a condição humana através de soluções baseadas em ciência nas áreas de clima, educação, saúde e equidade. O instituto realiza pesquisas multidisciplinares que abrangem áreas diversas como cuidados de saúde, desenvolvimento internacional, ciências ambientais e justiça social e econômica. O RTI International colabora com uma vasta gama de parceiros, incluindo governos, empresas, universidades e organizações sem fins lucrativos, para conduzir pesquisas e fornecer serviços técnicos. O objetivo é impactar o bem-estar global, aproveitando a expertise em áreas como soluções para mudanças climáticas, reforma educacional, saúde pública, segurança alimentar e mais. O RTI International também enfatiza a responsabilidade corporativa, sustentabilidade e compromisso com a qualidade e ética em suas operações.
🕒 Julho 17
🗣️🇺🇸🇬🇧 Inglês obrigatório
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

1001 - 5000 funcionários
Fundada em 1958
🏥 Saúde
💼 Consultoria
📦 Logística
Healthcare • Consulting • Logistics
O RTI International é um instituto de pesquisa independente sem fins lucrativos dedicado a melhorar a condição humana através de soluções baseadas em ciência nas áreas de clima, educação, saúde e equidade. O instituto realiza pesquisas multidisciplinares que abrangem áreas diversas como cuidados de saúde, desenvolvimento internacional, ciências ambientais e justiça social e econômica. O RTI International colabora com uma vasta gama de parceiros, incluindo governos, empresas, universidades e organizações sem fins lucrativos, para conduzir pesquisas e fornecer serviços técnicos. O objetivo é impactar o bem-estar global, aproveitando a expertise em áreas como soluções para mudanças climáticas, reforma educacional, saúde pública, segurança alimentar e mais. O RTI International também enfatiza a responsabilidade corporativa, sustentabilidade e compromisso com a qualidade e ética em suas operações.
• lead complex patient-centered outcomes research programs from study design through final delivery • serve as project lead for multidisciplinary teams, ensuring projects are delivered on time, within scope, and to the highest scientific standards • provide strategic oversight of study design, methodology, regulatory engagement, and evidence generation plans • manage project risks, client expectations, resource allocation, and team performance • personally contribute to the design, execution, analysis, interpretation, and reporting of qualitative and mixed-methods research studies • design and lead qualitative research conducted with patients, caregivers, patient advocates, and clinical key opinion leaders, including both stand-alone and clinical trial-based studies • lead the development, adaptation, and evaluation of clinical outcome assessments (COAs), including patient-reported outcomes (PROs), observer-reported outcomes (ObsROs), clinician-reported outcomes (ClinROs), and related measures • review and critically appraise published literature, COA development programs, and psychometric evidence • develop patient-centered evidence strategies to support regulatory, access & reimbursement, and healthcare decision-making needs • contribute directly to study reports, client presentations, evidence dossiers, briefing books, and negotiations with key decision makers to support patient-centered value messaging for medicines • build and maintain strong relationships with existing and prospective clients • lead scientific discussions with pharmaceutical and biotechnology sponsors regarding patient-focused drug development strategies • support business development efforts through proposal development, client meetings, capability presentations, and identification of growth opportunities • lead and contribute to scientific publications, conference abstracts, posters, presentations, and manuscripts
• postgraduate master’s level degree plus a minimum of 8 years of experience conducting patient-centered research, or a PhD plus a minimum of 5 years of experience conducting patient-centered research • demonstrated experience leading complex patient-centered research projects and multidisciplinary teams within a consulting, pharmaceutical, regulatory, CRO, or academic research environment supporting patient-focused drug development • demonstrated success managing client relationships, mentoring research staff, and leading project teams • substantial experience developing and successfully executing patient-centered evidence-generation strategies for pharmaceutical clients • proven experience interacting with regulatory agencies, including FDA, EMA, or other global health authorities as well as supporting evidence needs for access stakeholders (payers HTA, and prescribers) • experience leading proposal development and contributing to business growth initiatives • strong publication record and experience presenting research at scientific conferences.
• competitive base salary • generous paid time off policy • merit based annual increases • bonus opportunities • robust recognition program • competitive range of insurance plans (including health, dental, life, and short-term and long-term disability) • access to a retirement savings program such as a 401(k) plan • paid parental leave for all parents • financial assistance with adoption expenses or infertility treatments • financial reimbursement for education and developmental opportunities • employee assistance program • numerous other offerings to support a healthy work-life balance
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