Clinical Research Associate - Madrid: Trials Monitoring

Novo Nordisk; Madrid; On-site; EUR 42,000 - 74,000; Full time

Job summary

Novo Nordisk in Madrid, Spain is seeking a Clinical Research Associate to support clinical trials from site engagement through monitoring and data integrity. You will collaborate with Trial Managers and cross-functional teams to ensure patient safety and trial quality.

The role emphasizes proactive issue resolution, use of digital tools, and travel to sites as required. A Master’s in Life Sciences and relevant monitoring experience are essential to join this dynamic development centre.

Qualifications

• Master's degree in Life Sciences or related field.
• Experience in clinical trial monitoring or in a relevant pharma/CRO role.
• Strong knowledge of ICH-GCP, trial processes and regulatory requirements.
• Ability to deliver high-quality, compliant trial execution with patient safety and data integrity focus.
• Strong communication, collaboration and stakeholder management skills.

Responsibilities

• Partner with sites to understand needs, build relationships and drive actions to support recruitment, retention and milestones.
• Monitor trials according to study requirements, use data and risk insights to prioritize activities and resolve issues.
• Take ownership and collaborate with Trial Manager and team on shared decisions.
• Improve ways of working by using approved digital tools, sharing site insights and contributing to cross-trial initiatives.

Skills

Clinical trial monitoring

ICH-GCP knowledge

Data integrity

Communication

Stakeholder management

Willingness to travel

Education

Master's degree in Life Sciences

Job description

Novo Nordisk in Madrid, Spain is seeking a Clinical Research Associate to support clinical trials from site engagement through monitoring and data integrity. You will collaborate with Trial Managers and cross-functional teams to ensure patient safety and trial quality.

The role emphasizes proactive issue resolution, use of digital tools, and travel to sites as required. A Master’s in Life Sciences and relevant monitoring experience are essential to join this dynamic development centre.