Clinical Research AssociateVerified as a real position

Who we’re looking for

• A Master's degree in Life Sciences or a related field, combined with 2+ years' experience in clinical trial monitoring or a relevant pharmaceutical industry/CRO role
• Strong knowledge of ICH-GCP guidelines, regulatory requirements, and clinical trial methodology, with a demonstrated ability to ensure high-quality trial execution in compliance with internal SOPs
• Excellent stakeholder management, written and verbal communication skills, and a proven ability to build strong relationships with internal and external partners at all levels
• Strong organisational and project management capabilities, with high attention to detail, sound problem-solving and decision-making skills, and the ability to manage multiple sites and priorities independently and as part of a team
• Proficiency in digital tools including EDC, CTMS, and eTMF systems, an openness to embracing new technologies and better ways of working, and flexibility to travel as required

What you’ll do

• Overseeing and managing assigned clinical trial sites, conducting on-site and off-site monitoring visits in line with the Monitoring Plan, Protocol, ICH-GCP, internal SOPs, and applicable regulatory requirements
• Safeguarding patient safety and data integrity by monitoring site data, resolving discrepancies, and managing adverse events, while overseeing IP, study supplies, essential documents, and Investigator Trial Master File documentation
• Driving the implementation of Risk-Based Quality Management (RBQM) principles to proactively identify, assess, and mitigate risks, and maintaining inspection readiness throughout the trial
• Building and maintaining strong relationships with investigators and site staff, leading site training, and providing continuous support on protocols, systems, and compliance requirements
• Collaborating with Trial Managers, Study Start-up, Vendor Managers, and cross-functional teams to ensure alignment and smooth study execution
• Sharing site feedback and engagement insights to inform protocol updates, patient engagement initiatives, and continuous process improvement
• Acting as an ambassador for Novo Nordisk values at the site level

About the position

Clinical Research Associate Bring clinical trials to life at the sites where science meets patients – and help shape the therapies that will define the future of chronic disease care.

Benefits

• At Novo Nordisk, you’ll join a global healthcare company with a unique culture and strong results. We offer continuous learning, career development, and benefits tailored to your life and career stage.
• Salary: For this role, the Annual Base Salary ranges from 758,350.00 to 1,251,290.00 CZK, corresponding to the level of the position.
• The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience.
• Incentives and Benefits: The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.