Clinical Research Associate: Site Monitoring & Data Integrity

Novo Nordisk A/S; Puteaux; On-site; EUR 49,000 - 71,000; Full time

Benefits offered by this job

Incentives

Job summary

Novo Nordisk A/S in Paris, France, invites a Clinical Research Associate to oversee trial sites, ensure data integrity, and protect participant safety across monitoring activities. You will conduct on-site and remote visits, manage RBQM, review data, resolve discrepancies, and support audits while collaborating with investigators and cross-functional teams.

Annual base salary ranges from €49,200 to €71,340, with the placement based on skills and experience; incentives and benefits may be

Qualifications

• Bachelor’s degree in Life Sciences or a related field.
• 1+ years’ experience in clinical trial monitoring or related role.
• Strong knowledge of ICH-GCP guidelines and regulatory requirements.
• Excellent organizational, time management and project management skills.
• Proficiency with digital trial tools including EDC, CTMS and eTMF.
• Excellent written and verbal communication; ability to build relationships at all levels.
• Proactive problem-solving and risk identification abilities.
• Flexibility to travel to sites as required.
• Fluency in French and professional English.

Responsibilities

• Oversee assigned trial sites from monitoring through inspection readiness.
• Conduct on-site and remote monitoring visits per Monitoring Plan and regulatory requirements.
• Protect patient safety and data integrity by reviewing site data and resolving discrepancies.
• Track site performance, recruitment and retention, and address site issues early.
• Apply RBQM principles to identify and mitigate risks and support audits.
• Train sites on protocols and systems and manage investigational products and essential documents.
• Share insights to improve protocols, patient engagement and planning.

Skills

Bachelor’s degree

Trial monitoring

ICH-GCP

Organization

Digital tools

Communication

Problem solving

Travel-ready

FR/EN languages

Education

Bachelor’s degree in Life Sciences

Tools

EDC

CTMS

eTMF

Job description

Novo Nordisk A/S in Paris, France, invites a Clinical Research Associate to oversee trial sites, ensure data integrity, and protect participant safety across monitoring activities. You will conduct on-site and remote visits, manage RBQM, review data, resolve discrepancies, and support audits while collaborating with investigators and cross-functional teams.

Annual base salary ranges from €49,200 to €71,340, with the placement based on skills and experience; incentives and benefits may be