Clinical Data Reviewer

PSI CRO; São Paulo; Teletrabalho; BRL 50.000 - 70.000; Tempo integral

Resumo da oferta

A global clinical research organization in São Paulo is seeking a Clinical Data Monitor to ensure high-quality study data through effective monitoring. Responsibilities include reviewing data, identifying issues, and assisting with central monitoring tasks. The ideal candidate has a degree, experience in clinical research, and proficiency in English and Microsoft Office. This position offers remote work and opportunities for professional development.

Qualificações

• Prior experience in Clinical Research.
• Experience in central monitoring and clinical data review is a plus.
• Ability to learn, plan, and work in a dynamic team environment.

Responsabilidades

• Review EDC IxRS Laboratory and other vendors data.
• Identify single errors and systematic issues related to site performance.
• Generate follow-ups and resolve data queries and site issues.

Conhecimentos

Analytical mindset

Attention to detail

Full working proficiency in English

Proficiency in MS Office applications

Formação académica

College / University degree or equivalent

Descrição da oferta de emprego

You will join a widespread yet closely-knit team with the same mentality and desire to develop smart and intelligent approach to project monitoring. You will help to shape the future of effective risk-based monitoring at PSI and ensure higher quality of study data. You will spend time monitoring study data remotely identifying errors and issues with site performance.

Responsibilities

• Review EDC IxRS Laboratory and other vendors data and clinical listings
• Identify single errors and systematic issues related to site performance
• Generate follow up and resolves data queries and site issues
• Identify and record protocol deviations
• Assist to Central Monitoring Manager with administrative activities including managing study data documents and reports
• Ensuresite monitors receive information on site related risk & issues. Escalate findings to study teams
• Assists with root cause investigation and follow up on site performance signals identified during central monitoring review

Qualifications

• College / University degree or an equivalent combination of education training & experience
• Prior experience in Clinical Research
• Experience in central monitoring and clinical data review is a plus
• Full working proficiency in English
• Proficiency in MS Office applications
• Analytical mindset and attention to detail
• Ability to learn plan and work in a dynamic team environment

Additional Information

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

Remote Work: Yes

Employment Type: Full-time

Vacancy: 1