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Certified nursing assistant Jobs in Glace Bay, NS
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Certified nursing assistant • glace bay ns
- Promoted
Clinical Site Manager (Nursing Background)
Barrington JamesNova Scotia, Canada- Promoted
Administrative assistant
Randstad CanadaHalifax, Nova Scotia, CAMarketing Assistant Part-time
Top Level PromotionsCape Breton, NS, caAdministrative Assistant
PCL ConstructionCape Breton, Nova, CAStore Assistant Manager
Northern ReflectionsNova ScotiaPublic Relations Assistant
Hustle Notice BizHalifax, Nova Scotia, CAAssistant Manager
A&W Food Services of CanadaGlace Bay, NS, CARegistered Dental Assistant
Dentalcorp CanadaHalifax, Nova Scotia, CanadaRehab Assistant
Bayshore HealthCareNova ScotiaExecutive Assistant
Meridia Recruitment SolutionsNova ScotiaDental Assistant - Inventory
Treasury Board of Canada SecretariatHalifax, Nova ScotiaAssistant Resident Manager
Skyline Group of CompaniesHalifax, NS, CanadaPhysician Assistant - Primary Health Care
Nova Scotia Health and IWK HealthAll Locations, NS, CAAdministrative Assistant
CB CanadaHalifax, Nova Scotia, CanadaManager Assistant Store
SobeysHalifax, Nova Scotia, CARetail Assistant Manager
ShowcaseHalifax, Nova ScotiaPhysician Assistant - Primary Health Care
SuccessFactorsAll Locations, NS, CAClinical Site Manager (Nursing Background)
Barrington JamesNova Scotia, Canada- Temporary
40hours a week 12 month contract on a T4. Position is on site 5 days a week
A Clinical Site Manager with a nursing qualification in Canada typically oversees clinical trials, ensuring that research sites comply with regulations and study protocols. Their role combines clinical expertise with project management and regulatory compliance.
Job Description : Clinical Site Manager (Nursing Background)
Job Overview :
The Clinical Site Manager (CSM) is responsible for managing clinical trial sites, ensuring compliance with regulatory requirements, overseeing study protocols, and coordinating with healthcare professionals and sponsors. They play a crucial role in monitoring patient safety, data integrity, and site performance.
Key Responsibilities :
1. Site Management & Oversight
- Act as the primary liaison between the sponsor, contract research organization (CRO), and the clinical site.
- Ensure that clinical trials are conducted according to Good Clinical Practice (GCP), regulatory guidelines, and company SOPs.
- Conduct site visits for monitoring, risk assessment, and compliance verification.
- Resolve issues related to site performance, recruitment, and protocol adherence.
2. Patient Safety & Compliance
3. Regulatory & Documentation Compliance
4. Study Coordination & Training
5. Data Management & Reporting
Required Qualifications & Skills :
Education & Experience
Skills & Competencies
Work Environment :