
201 - 500 funcionários
💊 Farmacêutico
🏥 Saúde
💼 Consultoria
Pharmaceuticals • Healthcare • Consulting
Como uma CRO (Organização de Pesquisa por Contrato) especializada em dermatologia, fornecemos orientação científica, resultados precisos e satisfação do cliente. Nossa oferta de serviços única combina Serviços de Pesquisa Contratual especializados, conhecimento de locais de dermatologia na América do Norte e Europa e as capacidades ampliadas de um grande site de pesquisa clínica.
🕒 Setembro 8
🗣️🇺🇸🇬🇧 Inglês obrigatório
Melhore suas chances de conseguir uma entrevista verificando sua pontuação de currículo antes de se candidatar.

201 - 500 funcionários
💊 Farmacêutico
🏥 Saúde
💼 Consultoria
Pharmaceuticals • Healthcare • Consulting
Como uma CRO (Organização de Pesquisa por Contrato) especializada em dermatologia, fornecemos orientação científica, resultados precisos e satisfação do cliente. Nossa oferta de serviços única combina Serviços de Pesquisa Contratual especializados, conhecimento de locais de dermatologia na América do Norte e Europa e as capacidades ampliadas de um grande site de pesquisa clínica.
• Serve as the main point of contact for site selection activities, including site identification and feasibility • Develop and maintain positive and productive relationships with key clinical research sites • Identify investigators and research sites to expand the investigator database through literature and online searches • Collect information to define ideal investigators for studies • Identify and recommend potential investigators for studies • Develop interest survey assessments for studies • Create and coordinate distribution of study-specific feasibility questionnaires • Review completed feasibility questionnaires and recommend sites for qualification visits • Coordinate CRA resource allocation for site qualification visits • Review site qualification visit summaries • Recommend sites for study participation in consultation with the Sponsor and project team members • Track key site selection activities in the Clinical Trial Management System (CTMS) • Attend internal and external project team meetings as necessary • Identify site quality issues on active studies through project meetings, escalated site communications, and quality assurance audit findings • Participate in internal departmental projects related to site selection, contracting, and site intelligence • Support the Manager, Site Selection in understanding project goals, scope, and requirements and delivering high-quality results
• Bachelor’s degree in science or relevant field of study • Excellent oral and written skills in English; French is an asset • Minimum of 3 years of experience in clinical research in the biotechnology, pharmaceutical, or CRO industry • Significant and relevant experience in site selection, study start-up activities, site budget/contract negotiation and/or working closely with sites or in a site environment • Excellent knowledge of Microsoft Office suite (Word, Excel, Power Point) • Experience of dermatological clinical research is an asset • Ability to learn quickly, adapt, and work in a versatile environment • Ability to work in a team environment and establish good relationships with colleagues, sponsors, and sites • Organized, able to juggle competing priorities, and work in a fast-paced and evolving environment • Flexibility, positive attitude, superior attention to detail, and critical thinking skills • Good knowledge of good clinical practices and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines • Must be legally able to work in Germany
• Stimulating work environment • Attractive advancement opportunities • Home-based position in Germany • Equal opportunity and accommodations throughout the recruitment and selection process for applicants with disabilities, upon request
Candidatar-se🕒 Setembro 8
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