Medical Monitor, Certified Radio-Oncologist

PSI CRO; São Paulo; Teletrabalho; BRL 100.000 - 200.000; Tempo integral

Resumo da oferta

Join a forward-thinking Contract Research Organization that values both stability and innovation. As a Medical Monitor, you will play a crucial role in global clinical studies, ensuring the safety and well-being of patients. This position offers the opportunity to collaborate with diverse teams, review and analyze clinical data, and contribute to the development of new medications. With a strong emphasis on quality and timely service, this role is perfect for experienced Oncologists looking to make a significant impact in the medical field. Embrace a career that blends expertise with a passion for patient care.

Qualificações

• 10+ years of experience as a practicing Oncologist.
• Proficient in both English and Portuguese.

Responsabilidades

• Advise clients and teams on medical matters and ensure patient safety.
• Review clinical data for accuracy and compliance with protocols.

Conhecimentos

Oncology Fellowship certification

Communication skills

Analytical skills

Problem-solving skills

Proficiency in English

Proficiency in Portuguese

Team-oriented

Detail-oriented

Formação académica

Oncology Fellowship

Ferramentas

MS Office

Descrição da oferta de emprego

Medical Monitor, Certified Radio-Oncologist

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.

PSI Medical Monitors provide medical input to global clinical studies and advise teams and business partners, 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 preparing clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, manuscripts, and scientific presentations.
• Review and analyze clinical data to ensure the safety of study participants.
• Ensure reported data accuracy, completeness, and verifiability, and that trial conduct complies with the approved protocol/amendments.
• Address safety issues from sites and the study team.
• Review listings for coded events to verify Medical Dictionary for Regulatory Activities (MedDRA) coding.
• Assist in pharmacovigilance activities.
• Identify program risks and develop mitigation strategies with Clinical Operations.
• 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 on clinical documents with medical relevance.

Qualifications:

• Oncology Fellowship certification is mandatory.
• Minimum of 10 years' experience as a practicing Oncologist.
• Proficiency in English and Portuguese.
• Proficiency with MS Office applications.
• Strong communication, presentation, and analytical skills.
• Problem-solving skills, team-oriented, detail-oriented.

Joining PSI's Medical Monitoring team means becoming part of an international group of medical professionals, building a career at the forefront of medical science, and using your expertise to help bring new medications to patients in need.