Clinical Research Associate

ICON; Brasil; Teletrabalho; BRL 60.000 - 80.000; Tempo integral

Resumo da oferta

Join a leading global Biotechnology company as a Clinical Research Associate. You will be responsible for monitoring clinical trials, ensuring compliance with regulations, and protecting study participants. This role requires a Bachelor's degree and fluency in English and the host country language. ICON offers competitive salaries and a commitment to diversity and inclusion.

Serviços

Competitive Salary

Additional Benefits

Work-Life Balance Opportunities

Qualificações

• 1 year of on-site monitoring and study start-up experience.
• Experience in oncology is a plus.

Responsabilidades

• Completes onsite and remote monitoring activities following ICH-GCP guidelines.
• Ensures integrity of clinical data and compliance with protocols.
• Writes and submits reports of investigational site findings.

Conhecimentos

Negotiating Skills

Fluent English

Fluent Host Country Language

Formação académica

Bachelor’s degree in a health, life sciences or relevant field

Descrição da oferta de emprego

As Clinical Research Associate (CRA), you will be joining the world's largest & most comprehensive clinical research organization, powered by healthcare intelligence

You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies. They focus on areas with unmet medical need with the ambition to help reduce the social and economic burden of disease in society today.

What you will be doing:

• Completes onsite and remote monitoring activities in accordance with all ICH-GCP guidelines, applicable regulations, SOPs and study processes
• Verifies the protection of study participants by confirming informed consent procedures and protocol have been performed in accordance to applicable regulations.
• Ensures the integrity of clinical data and that the study is conducted in compliance with approved protocol, GCP, applicable regulations and SOPs.
• Writes and submits reports of investigational site findings and updates applicable tracking systems. Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate.
• Participates in audit preparation and follow-up activities as needed.
• May serve as preceptor, providing training to less experienced clinical team members.
• May be assigned clinical tasks where advanced negotiating skills are required.

You are:

• Bachelor’s degree in a health, life sciences or other relevant field of study.
• Previous experience supporting clinical trials including 1 year of on-site monitoring and study start up experience.
• Previous experience in oncology is a plus.
• Travel is required.
• All employees must read, write and speak fluent English and host country language.

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.