Location: Calgary, Alberta, CAClinical Research AssociateAre you passionate about clinical research and ensuring patient safety? Do you have a strong understanding of ICH‑GCP guidelines and enjoy collaborating with diverse stakeholders? If so, we invite you to join Novo Nordisk as a Clinical Research Associate. Take the next step in your career and help us drive high-quality clinical trials that make a difference.The positionAs a Clinical Research Associate at Novo Nordisk, you will:Oversee and manage assigned clinical trial sites, conducting on‑site and remote monitoring visits to ensure compliance with protocols, ICH‑GCP guidelines, and regulatory requirements.Drive the implementation of Risk‑Based Quality Management (RBQM) principles to proactively identify, assess, and mitigate risks throughout study conduct.Build and maintain strong relationships with investigators, site staff, and cross‑functional teams to support efficient clinical trial execution.Monitor site performance, recruitment progress, retention, and data collection to ensure study timelines and quality objectives are met.Ensure patient safety and data integrity by resolving discrepancies, managing adverse events, and maintaining inspection readiness.Provide site training and continuous support on study protocols, operational procedures, systems, and compliance requirements.Act as an ambassador for Novo Nordisk values at the site level, ensuring high‑quality trial execution.QualificationsBachelor’s degree in Life Sciences (or related field) minimum1+ years’ experience in clinical trial monitoring or a relevant pharmaceutical industry/CRO roleStrong understanding of ICH‑GCP, regulatory requirements,



and clinical trial methodologyDemonstrated ability to ensure high‑quality execution of clinical trial activities in compliance with ICH‑GCP, regulatory requirements, and internal SOPsAbility to build and maintain solid relationships with internal and external stakeholders across all organizational levelsExcellent written and verbal communication and stakeholder management skillsConfident working in dynamic environments independently and as part of a teamStrong organizational and time management skills, with the ability to manage multiple sites and prioritiesStrong project management capabilities with high attention to detail, integrity, and commitment to quality and patient safetyProficiency in digital tools, including EDC, CTMS, eTMF, and other clinical trial softwareStrong problem‑solving and decision‑making capabilities, including proactive risk identification and mitigationStrong attention to detail and commitment to high‑quality, compliant trial conductOpen to embracing better ways of working and continuous improvement, including new technologies and digital toolsUp to 70% travel required, in alignment with local Regional/CDC requirementsBenefitsSalary: For this role, the annual base salary ranges from $99,890–$149,890. The placement in the salary range will be assessed during the recruitment process based on your skills, competencies, and knowledge, and how your relevant experience matches the position requirements.Incentives: Based on the role’s level and other factors, the salary package may include short‑term (STI) and/or long‑term (LTI) incentives.Benefits: The eligibility for specific benefits may vary based on the job and location.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.#J-18808-Ljbffr

📌 Clinical Research Associate - C$99,890 - C$149,890 A Year (Winnipeg)
🏢 Novo Nordisk
📍 Winnipeg