Clinical Research Associate II / Senior CRA (Devices)

ICON Strategic Solutions; Brasil; Presencial; BRL 20.000 - 35.000; Tempo integral

Resumo da oferta

A leading clinical research organization in Brazil seeks a Clinical Research Associate to oversee and coordinate clinical trials, ensuring compliance with regulations and analyzing critical data. The role demands a Bachelor's degree in health or life sciences and on-site monitoring experience. Join a diverse team that prioritizes high performance and offers competitive benefits for work-life balance.

Serviços

Competitive salary

Range of additional benefits focused on well-being

Qualificações

• Bachelor's degree in health or life sciences required.
• Experience with on-site monitoring and CRA responsibilities.
• Familiarity with medical data evaluation and ICH-GCP guidelines.

Responsabilidades

• Coordinate clinical trial activities and maintain study documentation.
• Run sponsor queries efficiently and prepare study documentation.
• Develop relationships with stakeholders and site staff.
• Ensure compliance with procedures and patient safety.

Conhecimentos

Experience as CRA

On-site monitoring activities

Knowledge of ICH-GCP guidelines

Excellent written and verbal communication in English

Formação académica

Bachelor's degree in health, life sciences or related areas

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.

Responsibilities

• 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.

Qualifications

• 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

Inclusion & equal opportunity

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

Applicant note

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.