Clinical Data Reviewer

Psicro; São Paulo; Teletrabalho; BRL 60.000 - 80.000; Tempo integral

Resumo da oferta

Join a dynamic global company focused on medical science and project monitoring. As part of a closely-knit team, you will ensure the quality of study data through remote monitoring and data analysis. This role offers the opportunity to develop your skills in clinical research while contributing to meaningful projects that change lives.

Qualificações

• Prior experience in Clinical Research.
• Experience in central monitoring and clinical data review is a plus.

Responsabilidades

• Review EDC, IxRS, Laboratory, and other vendors’ data.
• Identify errors and systematic issues related to site performance.
• Assist with root cause investigations and follow-up on site performance signals.

Conhecimentos

Analytical mindset

Attention to detail

Full working proficiency in English

Formação académica

College/University degree

Ferramentas

MS Office

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 a smart and intelligent approach to project monitoring. You will help shape the future of effective risk-based monitoring at PSI and ensure higher quality of study data. Your role involves remote monitoring of study data, identifying errors and issues related to site performance.

Responsibilities

1. Review EDC, IxRS, Laboratory, and other vendors’ data and clinical listings.
2. Identify errors and systematic issues related to site performance.
3. Generate, follow up, and resolve data queries and site issues.
4. Identify and record protocol deviations.
5. Assist the Central Monitoring Manager with administrative activities, including managing study data, documents, and reports.
6. Ensure site monitors receive information on site-related risks and issues, and escalate findings to study teams.
7. Assist with root cause investigations and follow-up on site performance signals during central monitoring review.

Qualifications

1. College/University degree or equivalent education, training, and experience.
2. Prior experience in Clinical Research.
3. Experience in central monitoring and clinical data review is a plus.
4. Full working proficiency in English.
5. Proficiency in MS Office applications.
6. Analytical mindset and attention to detail.
7. Ability to learn, plan, and work effectively in a dynamic team environment.

Additional Information

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