Medical Monitor, Certified Radio-Oncologist

PSI CRO; São Paulo; Presencial; BRL 200.000 - 400.000; Tempo integral

Resumo da oferta

Uma organização de pesquisa clínica de renome está em busca de Monitores Médicos para fornecer orientação médica em estudos clínicos globais. Esta posição oferece a oportunidade de trabalhar em um ambiente colaborativo, onde você poderá aplicar seu conhecimento em Oncologia e contribuir para a segurança e bem-estar dos pacientes. Com mais de 25 anos de experiência, a empresa combina estabilidade e inovação, permitindo que você desenvolva sua carreira na vanguarda da ciência médica. Se você é um médico experiente em Oncologia e busca um papel impactante, esta é a oportunidade ideal para você.

Qualificações

• Médico com experiência em Oncologia e fluência em inglês e português.
• Habilidades em comunicação e análise de dados clínicos são essenciais.

Responsabilidades

• Aconselhar equipes sobre questões médicas e garantir a segurança dos participantes.
• Revisar e analisar dados clínicos para conformidade com protocolos.

Conhecimentos

Habilidades de Comunicação

Habilidades de Apresentação

Habilidades Analíticas

Resolução de Problemas

Orientação para Detalhes

Formação académica

Diploma de Médico

Certificação de Fellowship em Oncologia

Ferramentas

MS Office

Descrição da oferta de emprego

Company Description

PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being.

Home-Based in Brazil

Responsibilities:

• Advise clients, project teams, sites, data safety monitoring boards, regulatory agencies and third-party vendors on medical matters
• Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and different scientific presentations
• Review and analyze clinical data to ensure the safety of study participants in clinical studies
• Ensure that the reported data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments
• Address safety issues across the study from sites and the study team
• Review listings for coded events to verify Medical Dictionary for Regulatory activities
• Participate in bid defense meetings
• Assist in Pharmacovigilance activities
• Identify Program risks, and create and implement mitigation strategies with Clinical Operations
• Ability to organize and lead clinical development advisory boards and safety monitoring boards
• Ensure Study team compliance with FDA, EMEA, ICH and GCP guidelines
• Review and sign off clinical documents with respect to medical relevance.

Qualifications

• Medical Doctor degree
• Oncology Fellowship certification is a must
• Prior and wide experience as a practicing Oncologist (minimum of 10 years)
• Full working proficiency in English and Portuguese
• Proficiency with MS Office applications
• Communication, presentation and analytical skills
• Problem-solving, team and detail-oriented

As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.