Medical Monitor, Certified Radio-Oncologist

PSI CRO; Ciudad de México; Presencial; MXN 600,000 - 1,000,000; Jornada completa

Descripción de la vacante

Una organización de investigación clínica líder busca un Monitor Médico con un enfoque en la seguridad del paciente y el bienestar. Este papel crucial implica asesorar a equipos de proyectos y agencias regulatorias, colaborando en el desarrollo de planes clínicos y garantizando la precisión de los datos. Con más de 25 años en la industria, esta firma innovadora ofrece un entorno de trabajo dinámico donde los profesionales médicos pueden crecer y contribuir a la ciencia médica. Si tienes una sólida experiencia en oncología y un deseo de marcar la diferencia, esta es la oportunidad ideal para ti.

Formación

• Médico con experiencia en oncología y habilidades de comunicación efectivas.
• Certificación en oncología y dominio del inglés y español son imprescindibles.

Responsabilidades

• Asesorar sobre asuntos médicos a equipos de proyectos y reguladores.
• Revisar datos clínicos para garantizar la seguridad de los participantes.

Conocimientos

Habilidades de comunicación

Habilidades de presentación

Habilidades analíticas

Resolución de problemas

Orientación al detalle

Educación

Título de Médico

Certificación de Fellowship en Oncología

Herramientas

MS Office

Descripción del empleo

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 Mexico

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 analysis of 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 Spanish
• 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.