Clinical Data Reviewer

PSI CRO AG; São Paulo; Presencial; BRL 40.000 - 60.000; Tempo integral

Resumo da oferta

PSI CRO AG recherche un membre de l'équipe de surveillance clinique pour améliorer la qualité des données d'étude. En rejoignant une équipe dynamique, vous serez impliqué dans le suivi des performances des sites et la gestion des données cliniques. Ce rôle exige une attention aux détails et une maîtrise de l'anglais, avec une formation universitaire requise. Rejoignez une entreprise qui investit dans le développement professionnel et le succès de ses employés.

Serviços

Opportunités de développement professionnel

Qualificações

• Expérience préalable en recherche clinique.
• Expérience en surveillance centrale et revue de données cliniques appréciée.
• Capacité à apprendre et à travailler dans un environnement dynamique.

Responsabilidades

• Revoir les données des vendeurs et identifier les erreurs de performance du site.
• Gérer les requêtes de données et les problèmes de site.
• Assister le Central Monitoring Manager avec les activités administratives.

Conhecimentos

Analytical mindset

Attention to detail

Full working proficiency in English

Formação académica

College/University degree or equivalent

Ferramentas

MS Office applications

Descrição da oferta de emprego

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

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.

You will:

• 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.