Clinical Research Associate — Site-Focused Monitoring

Novo Nordisk A/S; Madrid; On-site; EUR 43,000 - 74,000; Full time

Job summary

Novo Nordisk A/S is seeking a Clinical Research Associate for the Clinical Development Centre Spain in Madrid. You will partner with trial sites to deliver quality, pace and patient-centred trials, ensuring regulatory compliance and data integrity throughout the study lifecycle.

You’ll work closely with Trial Managers and cross-functional teams to manage site relationships, monitor visits, and drive recruitment, retention and trial milestones in a dynamic environment.

Qualifications

• Master’s degree in Life Sciences or related field.
• Experience in clinical trial monitoring or related pharmaceutical/CRO role.
• Strong knowledge of ICH-GCP, regulatory requirements and trial processes.
• Ability to deliver high-quality, compliant trial execution with focus on patient safety and data integrity.

Responsibilities

• Partner with sites: understand their needs and drive actions to support recruitment, retention and milestones.
• Protect patients and trial quality: monitor according to study requirements and use risk insights to prioritise activities.
• Take ownership and collaborate: anticipate challenges and align with Trial Manager and team for decisions.
• Improve how we work: utilise approved digital tools, share insights, and contribute to cross-trial initiatives.

Skills

Clinical trial monitoring

ICH-GCP knowledge

Regulatory know-how

Data integrity

Stakeholder management

Education

Master’s degree in Life Sciences or related field

Job description

Novo Nordisk A/S is seeking a Clinical Research Associate for the Clinical Development Centre Spain in Madrid. You will partner with trial sites to deliver quality, pace and patient-centred trials, ensuring regulatory compliance and data integrity throughout the study lifecycle.

You’ll work closely with Trial Managers and cross-functional teams to manage site relationships, monitor visits, and drive recruitment, retention and trial milestones in a dynamic environment.