Clinical Research Associate 2 / SR CRA - FSO Model - Home Based Portugal

Fortrea; Portugal; Híbrido; EUR 30 000 - 50 000; Tempo integral

Resumo da oferta

A global clinical research organization is seeking a Clinical Research Associate (CRA) to manage trial sites and ensure data quality. You will play a critical role in clinical trials, requiring a degree in life sciences and strong attention to detail. The ideal candidate has oncology experience and is fluent in Portuguese and English. This position offers flexible work conditions and a commitment to employee well-being.

Serviços

Flexible work model

Competitive benefits

Professional development opportunities

Qualificações

• Experience in the oncology therapeutic area is a must.
• Solid understanding of ICH-GCP guidelines and local regulatory requirements.
• Fluent in Portuguese and English, both written and verbal.

Responsabilidades

• Manage clinical trial sites following SOPs and sponsor requirements.
• Conduct site monitoring visits ensuring safety and data integrity.
• Collaborate with teams to align site performance with study metrics.

Conhecimentos

Attention to detail

Clinical monitoring

Regulatory compliance

Technical proficiency

Formação académica

University or college degree in life sciences

Descrição da oferta de emprego

Be the connection between science and solutions.

In this CRA position, you’ll help transform complex clinical protocols into real-world results, working alongside a team that values precision, integrity, and progress. This role will offer you the opportunity to directly influence the success of global clinical trials and the delivery of innovative therapies to patients worldwide.

Key Responsibilities:

• Manage clinical trial sites in alignment with Fortrea SOPs, ICH-GCP, project plans, and sponsor requirements, including oversight of training documentation and regulatory compliance.
• Conduct all phases of site monitoring visits (pre-study, initiation, routine, and close-out), ensuring subject safety, protocol adherence, and data integrity.
• Perform source data verification, query resolution, and eCRF review to ensure high-quality, audit‑ready clinical data.
• Maintain and update essential documents in eTMF and sponsor systems, ensuring regulatory and documentation completeness throughout the study lifecycle.
• Monitor investigational product (IP) accountability, storage, and compliance with protocol and regulatory standards.
• Collaborate with cross‑functional teams to align site performance with study timelines, metrics, and quality expectations.

Required Qualifications:

• University or college degree in life sciences, nursing, pharmacy, or a related allied health profession; equivalent relevant experience may be considered in lieu of formal education.
• Experience in oncology therapeutic area.
• Solid understanding of ICH‑GCP guidelines and local regulatory requirements governing clinical research.
• Working knowledge of clinical trial processes and monitoring procedures.
• Strong attention to detail and ability to follow complex protocols and documentation standards.
• Fluent in Portuguese and in English both written and verbal.
• Proficient in using clinical systems and tools; able to work independently and travel as required.

Why Join Us?

• Contribute to advancing innovative therapies and improving patient outcomes through meaningful clinical research on a global scale.
• Thrive in a collaborative environment that values continuous learning, mentorship, and professional development.
• Work with modern clinical technologies and streamlined systems that support efficiency, quality, and compliance.
• Benefit from a flexible work model, competitive benefits, and a strong commitment to employee well‑being.

We invite qualified candidates who are committed to excellence in clinical research to apply and become part of Fortrea’s mission to advance healthcare worldwide. If you are seeking a rewarding opportunity within a globally respected organization, we encourage you to submit your application today.

Learn more about our EEO & Accommodations request here.