In-House CRA

ICON Strategic Solutions; Brasil; Presencial; BRL 30.000 - 60.000; Tempo integral

Resumo da oferta

Join a leading clinical research organization as an In-House CRA/CTA, where you will play a pivotal role in supporting clinical studies. This position offers a unique opportunity to engage with sites and investigators, ensuring the smooth operation of clinical trials. You will conduct remote management activities, maintain professional relationships, and uphold the highest standards of confidentiality. With a focus on diversity and inclusion, this organization values high performance and nurtures talent, making it an ideal place for career growth and development. If you are passionate about clinical research and eager to make a difference, this role is perfect for you.

Qualificações

• Bachelor's degree in health, life sciences or related fields required.
• Experience in clinical research and ethics submissions is essential.

Responsabilidades

• Serve as the primary in-house contact for sites and investigators.
• Conduct remote site management activities according to SOPS.
• Maintain confidentiality and participate in QA audits as needed.

Conhecimentos

Clinical Research

ICH-GCP Compliance

Data Management

Communication Skills

Problem Solving

Formação académica

Bachelor's Degree in Health or Life Sciences

Descrição da oferta de emprego

As an In-House CRA/CTA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing:

• Serve as the primary in-house contact for sites and investigators participating in studies.
• Conducts and completes remote site management activities, with support as needed, according to applicable SOPS and the Study Monitoring Plan.
• To contact Clinical sites for specific requests (e.g. enrolment updates, missing documentation, data entry timeliness, data query follow-up, CDA finding follow-up, and action Item resolution or other sponsor specific CRA tasks.
• Takes responsibility for project tasks and sees these tasks through to successful completion, with support.
• Maintains a professional interpersonal relationship with study team, sites, and Sponsor.
• Participates in QA Audits as needed.
• Regularly attends and contributes to project specific and departmental meetings.
• Maintains Sponsor and patient confidentiality.

• Bachelor's degree in health, life sciences or related fields.
• Experience in clinical research providing support for the studies and ethics submissions.
• Comprehensive knowledge and understanding of ICH-GCP and other relevant regulations for the conduct of clinical trials related to pharmaceuticals, biologics, medical devices and combination products.
• Good English level (conversation and writting) and Fluent Portuguese.
• Based in São Paul or greater São Paulo region.

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.