Clinical Research Associate II / Senior CRA (Devices)

ICON; Brasil; Presencial; BRL 30.000 - 45.000; Tempo integral

Resumo da oferta

A global leader in clinical research is looking for a Clinical Research Associate in Brazil. You will oversee clinical trials, ensuring compliance and data accuracy while maintaining strong relationships with stakeholders. A Bachelor's degree in health or life sciences and experience in on-site monitoring are required. Competitive salary and benefits focused on well-being are offered.

Serviços

Competitive salary

Benefits focused on well-being

Qualificações

• Experience as CRA with on-site monitoring activities, preferably with studies for medical devices.
• Knowledge of ICH-GCP guidelines and ability to review medical data.
• Excellent written and verbal communication in English.

Responsabilidades

• Coordinate all activities for setting up and monitoring clinical studies.
• Complete study status reports and maintain study documentation.
• Ensure compliance with regulations and company procedures.

Conhecimentos

Coordination of clinical trials

Excellent communication

On-site monitoring

Formação académica

Bachelor's degree in health or life sciences

Descrição da oferta de emprego

Overview

We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; you will also participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
• Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensure patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements.

• Bachelor\'s degree in health, life sciences or related areas.
• Experience as CRA and with on-site monitoring activities, preferably with studies for medical devices.
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
• Excellent written and verbal communication in English

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.