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Novo Nordisk

Clinical Research Associate 2

Novo Nordisk

Clinical Research Associate II at Novo Nordisk overseeing trial sites for clinical studies. Ensuring compliance and driving quality in clinical trials for serious chronic diseases like obesity and diabetes.

Posted 7/8/2026full-timeRoma • 🇮🇹 ItalyJuniorMid-Level💰 €43,940 - €68,110 per yearWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Provide strategic oversight and management of clinical trial sites
  • Ensure protocol compliance, data integrity, and the protection of patient safety and rights
  • Drive study quality and performance through risk-based monitoring and proactive risk management
  • Collaborate with site staff and cross-functional teams to ensure the successful execution of trials
  • Act as a Site Manager and build trusted partnerships with investigators and site staff
  • Conduct on-site and remote visits in accordance with the Monitoring Plan, Protocol, ICH-GCP, internal SOPs and regulatory requirements
  • Drive the implementation of Risk-Based Quality Management (RBQM) principles
  • Oversee site performance, recruitment progress, retention and data collection
  • Manage IMP, study supplies, essential documents and the Investigator Trial Master File

Requirements

What you’ll need
  • A bachelor's degree in Life Sciences (preferably Biotechnology, Pharmacy, Chemistry, Biology or CTF)
  • A minimum of 3 years of clinical trial monitoring experience within the pharmaceutical industry or a CRO
  • Proven independence in monitoring activities and strong expertise in applying ICH-GCP E6(R3), clinical trial methodology, regulatory requirements, and SOPs
  • Valid GCP certification required
  • Solid working knowledge of electronic clinical trial systems, including CTMS, EDC, IWRS and eTMF
  • Demonstrated digital mindset and willingness to actively leverage AI tools and emerging technologies to improve monitoring efficiency, data quality, and operational excellence
  • Excellent stakeholder management, communication and negotiation skills
  • Fluency in both Italian and English (written and spoken)
  • Flexibility to travel on a monthly basis

Benefits

Comp & perks
  • Continuous learning
  • Career development
  • Employee benefits tailored to life and career stage

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
Clinical Trial MethodologyRisk-Based Quality Management (RBQM)Data Collection ManagementProtocol CompliancePatient Safety Oversight
Soft Skills
Communication SkillsNegotiation SkillsStakeholder Management
Certifications
GCP Certification