Clinical Research Associate 2 - Home Based Barcelona / Madrid

Fortrea; Málaga; A distancia; EUR 40.000 - 55.000; Jornada completa

Descripción de la vacante

A leading clinical research organization is hiring a Clinical Research Associate 2 to support oncology and cardiovascular trials. This position offers home-based flexibility within Spain, specifically in Barcelona and Madrid. Candidates should have at least 1.5 years of clinical monitoring experience and a strong grasp of regulatory compliance. This is an opportunity to shape the future of clinical research while contributing to meaningful patient treatments.

Servicios

Comprehensive benefits package

Health and wellness programs

Opportunities for professional growth

Flexible work arrangements

Formación

• Minimum 1.5 years of clinical monitoring experience, especially in Oncology and Cardiovascular.
• Strong knowledge of ICH GCP guidelines.
• Proven site management skills and registry administration experience.

Responsabilidades

• Oversee site activities to ensure compliance.
• Conduct site monitoring visits and verify data accuracy.
• Ensure regulatory compliance and safeguard data integrity.
• Manage study documentation and investigational product accountability.

Conocimientos

Clinical monitoring experience

Knowledge of regulatory processes

Site management

Fluent in English

Descripción del empleo

Clinical Research Associate 2 - Home Based Barcelona / Madrid

Fortrea Madrid, Community of Madrid, Spain

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Join to apply for the Clinical Research Associate 2 - Home Based Barcelona / Madrid role at Fortrea

Clinical Research Associate 2 - Home Based Barcelona / Madrid

Fortrea Madrid, Community of Madrid, Spain

Join to apply for the Clinical Research Associate 2 - Home Based Barcelona / Madrid role at Fortrea

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Join Fortrea as a Clinical Research Associate (CRA2) – Drive Clinical Excellence in Oncology / Cardiovascular Trials.

Job Overview

We are looking for a CRA I / CRA II to join our FSP team in Barcelona and Madrid :

You will ensure clinical studies are conducted to the highest regulatory and quality standards, protecting patient safety and delivering reliable data. You’ll have the autonomy to manage sites and drive study outcomes while contributing to innovative research in critical therapeutic areas. Your work will help shape the future of clinical research and provide life-changing treatments to patients worldwide.

Summary Of Responsibilities

• Lead Site Management : You will oversee site activities to ensure compliance with ICH GCP guidelines, study protocols, and sponsor requirements.
• Conduct Site Monitoring Visits : Manage pre-study, initiation, routine, and close-out visits to verify data accuracy and study progress.
• Ensure Regulatory Compliance : Confirm informed consent procedures, monitor adverse events, and ensure site readiness for audits.
• Safeguard Data Integrity : Perform meticulous source document reviews and eCRF verifications to ensure data accuracy and resolution of queries.
• Manage Study Documentation : Maintain complete, current site regulatory documents and eTMF / Sponsor records throughout the trial.
• Investigational Product Accountability : Monitor investigational product inventory and secure storage per protocol.
• Drive Study Timelines : Align site activities with key milestones to meet critical project deliverables efficiently.

Qualifications

1.5 years of clinical monitoring experience, including Oncology and Cardiovascular therapeutic areas for minimum 1 year.

Strong knowledge of regulatory and drug development processes.

Advanced site monitoring, site management, and registry administration skills.

Fluent in local language and English, with excellent written and verbal communication.

Work Environment

60-80% overnight travel, valid driver’s license required.

Benefits

At Fortrea, we value our team members and offer a comprehensive benefits package, including competitive compensation, health and wellness programs, and opportunities for professional growth. You’ll also enjoy flexible work arrangements and the chance to make a meaningful impact in cutting-edge clinical research.

Your Contribution To Fortrea’ s Success

In this role, you will help ensure the smooth execution of clinical trials and play a key role in delivering high-quality data and compliance. Your efforts will contribute directly to Fortrea’s mission of advancing clinical research and improving global health outcomes. Ready to make an impact? Join us!

Learn more about our EEO & Accommodations request here. Seniority level

Seniority level Entry level

Employment type

Employment type Full-time

Job function

Job function Research, Analyst, and Information Technology

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