Senior Clinical Research Associate - CNS / Oncology - Spain - Remote

Worldwide Clinical Trials; Barcelona; A distancia; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading company in clinical research is looking for a Senior Clinical Research Associate to join their remote team in Spain. The role involves conducting site visits, ensuring compliance, and managing documentation across various therapeutic areas. Ideal candidates will have a degree in life sciences and at least two years of monitoring experience, along with strong communication and organizational skills.

Formación

• Minimum two years of independent clinical monitoring experience.
• Experience handling multiple protocols across therapeutic areas.
• Ability to travel as required.

Responsabilidades

• Conduct site visits: qualification, initiation, monitoring, management, and close-out.
• Review safety information and conduct source verification for compliance.
• Manage regulatory and ethical documentation.

Conocimientos

Communication

Organizational Skills

Clinical Research Principles

Proficiency in Microsoft Office

CTMS

EDC Systems

Educación

Four-year degree in life sciences

Descripción del empleo

Senior Clinical Research Associate - CNS / Oncology - Spain - Remote

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Who We Are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, a global team of over 3,500+ experts, bright thinkers, dreamers and doers, dedicated to changing how the world experiences CROs. Our mission is to work with passion and purpose daily to improve lives, and we seek others who share this pursuit.

Why Worldwide

We believe everyone plays a vital role in making a difference for patients and caregivers. From accessible leadership to supportive teams, we foster a diverse and inclusive environment that promotes collaboration and creativity. Our workplace encourages authenticity and inspires excellence. Join us!

What Clinical Operations Does at Worldwide

Within Clinical Operations, your contributions will impact patients' lives. As a CRA, you will work across therapeutic areas such as Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases, collaborating with top-tier colleagues. You will receive support in regulatory submissions, TMF management, and site management. We prioritize professional development through regular coaching, clear career paths, and accessible leadership, aiming to advance science and improve patient outcomes globally.

Responsibilities

1. Conduct site visits: qualification, initiation, monitoring, management, and close-out.
2. Review safety information, informed consent, and conduct source verification for compliance and data integrity.
3. Participate in study team and investigator meetings.
4. Manage regulatory and ethical documentation, review study materials.

Qualifications

• Excellent communication skills in English and local language.
• Strong organizational skills and ability to work independently.
• Understanding of clinical research principles and processes.
• Proficiency in Microsoft Office, CTMS, and EDC systems.

Experience

• Minimum two years of independent clinical monitoring experience.
• Experience handling multiple protocols across therapeutic areas.
• Four-year degree in life sciences or equivalent education/training.
• Ability to travel as required.

We are committed to diversity and inclusion, providing equal opportunities for all employees and applicants regardless of background or identity. Join us to make a difference and grow your career in clinical research.