Cra Ii

Intrials Clinical Research; Brasília; Híbrido; BRL 80.000 - 120.000; Tempo integral

Resumo da oferta

A clinical research organization is seeking a CRA II located in São Paulo, Brazil. The ideal candidate will have a degree in Health Sciences and at least 2 years of experience in clinical research. Responsibilities include ensuring compliance with guidelines, monitoring clinical studies, and acting as the primary contact for study sites. Knowledge of ICH-GCP and English proficiency are essential, while basic Spanish is a plus. This position offers a hybrid work model with significant travel opportunities.

Qualificações

• At least 2 years of experience in clinical research as a CRA at a CRO or pharmaceutical company.
• Knowledge of ICH-GCP and local/international guidelines.
• Able to travel considerably and manage travel schedules.

Responsabilidades

• Ensure clinical study compliance with guidelines and regulations.
• Perform monitoring activities on-site and remotely.
• Act as main point of contact for study sites.

Conhecimentos

Organizational abilities

Interpersonal relationships

Problem-solving

Self-confidence

Advanced English

Formação académica

Degree in Health Sciences or equivalent

Ferramentas

Microsoft Office

Descrição da oferta de emprego

CRA II

Location: São Paulo - São Paulo - Brazil

Hybrid (Vila Olimpia)

Who We Are

Intrials is a disruptive company with all the attributes that a CRO must master. We mix innovative projects with the necessary skills to provide a full service. Nothing stops us in the search for knowledge. Transforming people's lives through science when it comes to solving the challenges of our clients' projects in a focused and exclusive fashion.

Diversity & Inclusion are essential to continue building our history of innovation. Diversity of color, belief, sexual orientation, religion, or any other characteristic are very welcome in all open positions at our company. It is a fundamental part of Intrials to constantly think and implement actions that reinforce the importance of good coexistence with all the people who are part of our DNA and together, to leverage and build true impactful results in our society.

Basic Functions and Responsibilities includes, but are not limited to:

Ensure that the clinical study is conducted according to the ICH-GCP guidelines, the local and international regulations as well as according to Intrials or Sponsor's SOPs; Ensure that clinical study data are accurate and verifiable; Identify and perform the corresponding quality controls on source documents; Perform monitoring activities and visits (on-site and / or remote) : Site Selection Visit (SSV), Site Initiation Visits (SIV), Interim Monitoring Visit (IMV) and Close-out Visit (COV); Participate in meetings / teleconferences with Sponsor and PM; Act as main point of contact for study sites; Provide support to PM and more experienced CRAs in the study coordination activities, as applicable; Perform coaching activities for less experienced CRAs.

What you need:

• Degree in Health Sciences or equivalent (Pharmacy, Biology, Biomedicine, Nursing, other)
• Reliable academic background and at least 2 years of experience in clinical research as a CRA at CRO, or pharmaceutical company
• Excellent organizational abilities and interpersonal relationships; oriented to solve problems; self-confidence
• Available to travel considerably and ability to manage travel schedules
• Knowledge of ICH-GCP, local and international guidelines; Computer skills on Windows environment and Microsoft Office tools
• Advanced knowledge of English

Basic Spanish is recommended (only applicable for CRAs from Brazil).