Country Clinical Quality Manager
2 weeks ago
Fortrea (Nasdaq: FTRE) is a global clinical research organization (CRO) specializing in delivering innovative clinical development solutions for the life sciences industry. With over 30 years of clinical research expertise, Fortrea emerged from Covance and Labcorp, focusing on supporting biotech, biopharma, medical devices, and diagnostics. Operating in roughly 100 countries, Fortrea has extensive experience across more than 20 therapeutic areas, offering Phase I–IV clinical trial management, clinical pharmacology, and consulting services. The company's diverse and talented team leverages scientific rigor, operational excellence, and a strong investigator site network to deliver exceptional solutions, transforming aspirations into outcomes. Role Description Full‑time, on‑site role located in Kirkland, QC, for a Country Clinical Quality Manager. The manager will oversee quality and compliance activities within clinical trials, ensuring adherence to company policies, local regulations, and global standards. Responsibilities The role includes managing audit readiness, identifying and resolving quality issues, collaborating with cross‑functional teams, guiding process improvements, and supporting risk‑management strategies to ensure the delivery of high‑quality trial outcomes. Qualifications Strong knowledge of clinical trial quality management, compliance standards, and regulatory requirements. Experience in conducting audits, monitoring risk‑management processes, and implementing quality improvement initiatives. Proficiency in clinical trial processes, document review, and identifying regulatory trends. Excellent interpersonal and communication skills for cross‑functional collaboration and stakeholder management. Ability to lead projects independently, manage tasks proactively, and solve problems efficiently. Knowledge of therapeutic areas and experience working within the life sciences or CRO industry is preferred. Bachelor's degree in Life Sciences, Healthcare Management, or a related field; advanced degree is an advantage. Seniority Level Mid‑Senior level Employment Type Full‑time Location Kirkland, QC, Canada #J-18808-Ljbffr
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Country Clinical Quality Manager
1 week ago
Kirkland, Quebec, Canada Fortrea Full time $60,000 - $120,000 per yearCompany DescriptionFortrea (Nasdaq: FTRE) is a global clinical research organization (CRO) specializing in delivering innovative clinical development solutions for the life sciences industry. With over 30 years of clinical research expertise, Fortrea emerged from Covance and Labcorp, focusing on supporting biotech, biopharma, medical devices, and...
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Country Clinical Quality Manager Audit
2 weeks ago
Kirkland, Canada Fortrea Full timeA global clinical research organization is seeking a Country Clinical Quality Manager in Kirkland, QC. This full-time, on-site role involves overseeing quality compliance in clinical trials, managing audits, and supporting process improvements. The ideal candidate will have a bachelor's degree in Life Sciences, knowledge of regulatory standards, and the...
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Clinical Research Associate Manager
3 days ago
Kirkland, Canada Merck Sharp & Dohme Full time**Clinical Research Associate Manager** **Location: Based in British Columbia or Alberta** This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director or Head of Site Management and Monitoring, the person is responsible to manage a team of 6-14 Clinical Research Associates and to ensure...
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Kirkland, Canada IQVIA LLC Full timeResponsable des opérations cliniques, Manager, Clinical Operations page is loaded## Responsable des opérations cliniques, Manager, Clinical Operationslocations: Kirkland, Quebec, Canada: Mississauga, Ontario, Canadatime type: Full timeposted on: Posted Todayjob requisition id: R1513070Aperçu du posteGérer une équipe de personnel clinique...
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Kirkland, Canada IQVIA LLC Full timeResponsable des opérations cliniques, Manager, Clinical Operations page is loaded## Responsable des opérations cliniques, Manager, Clinical Operationslocations: Kirkland, Quebec, Canada: Mississauga, Ontario, Canadatime type: Full timeposted on: Posted Todayjob requisition id: R1513070Aperçu du posteGérer une équipe de personnel clinique...
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Kirkland, Canada IQVIA Full timeIQVIA Biotech partners exclusively with biotech and emerging biopharma companies to support clinical development across all phases and therapeutic areas. While we operate independently from IQVIA at large, we offer the same global reach, advanced technologies, and benefits. Our agile structure, collaborative culture, and deep scientific expertise allow us to...
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Study Operations Manager Ii
3 days ago
Kirkland, Canada Pfizer Full timeJob Summary The Study Operations Manager is responsible for study and regional/country level activities from study startup through conduct and study close. The Study Operations Manager will be assigned one or more studies and will be tasked with taking on several responsibilities in support of the larger Study Management deliverables. The Study Operations...
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Kirkland, Canada IQVIA Full timeAperçu du poste Gérer une équipe de personnel clinique travaillant à l’appui des études cliniques pour garantir que les projets disposent des ressources appropriées et que les employés soient formés et atteignent les objectifs du projet. Fonctions essentielles Gérer le personnel conformément aux politiques de l’organisation et aux règlements...
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Kirkland, Quebec, Canada IQVIA Full time $90,000 - $120,000 per yearAperçu du posteGérer une équipe de personnel clinique travaillant à l'appui des études cliniques pour garantir que les projets disposent des ressources appropriées et que les employés sont formés et atteignent les objectifs du projet.Fonctions essentielles• Gérer le personnel conformément aux politiques de l'organisation et aux règlements...
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Clinical Research Associate
1 week ago
Kirkland, Canada Novasyte Full timeJob Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...
