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Clinical Research Nurse
Altasciences. Oversee the safety and consent of clinical trial participants during study conduct .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in overseeing clinical trial participant safety and consent, executing compliance with Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs), and maintaining confidentiality. Proficient in administering Investigational Products (IP) and performing safety monitoring while effectively communicating with team members and managing multiple priorities.
Highest-signal resume keywords
Registered Nurse CertificationGood Clinical Practices (GCP)Investigational Product AdministrationBilingual Communication (French and English)Patient Care and Safety Advocacy
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Trial OversightSafety MonitoringEmergency Equipment InspectionCatheter InstallationAdverse Event DocumentationStudy Protocol ComplianceParticipant ScreeningRecord MaintenanceTask ExecutionConflict Management
Soft Skills
Excellent Communication SkillsInterpersonal SkillsCustomer Service FocusIntegrity and DiscretionAbility to Manage Priorities
Tools & Technologies
Microsoft Suite
Certifications & Qualifications
DEC from Accredited Registered Nurse ProgramPermit from Ordre des Infirmiers et Infirmières du Québec (OIIQ)
Industry Keywords
Clinical TrialsGood Clinical Practices (GCP)Standard Operating Procedures (SOPs)Patient ConfidentialitySafety Assessments
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Oversee the safety and consent of clinical trial participants during study conduct
- Maintain safety equipment
- Execute tasks in compliance with study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs)
- Perform scheduled inspection of emergency crash carts and maintain up-to-date records
- Ensure confidentiality of clinical trial participants and sponsors
- Perform continuous safety monitoring and safety assessments
- Administer Investigational Products (IP)
- Install catheters
- Monitor, document and/or follow up on participant adverse events
- Maintain and advocate patient care, quality, and safety
- Assist with study-related consenting and participant screenings
- Provide feedback on study progress
- Communicate issues and problem resolutions to supervisors and managers
- Train employees on clinical trial activities
- Complete other tasks assigned by management
Requirements
What you’ll need- DEC from accredited Registered Nurse program required
- Permit from the Ordre des infirmiers et infirmières du Québec (OIIQ) required
- Good communication in French and English
- Customer service focused
- Able to work in fast-paced environment
- Knowledge of the Microsoft suite
- Excellent verbal and written communication skills
- Well-developed interpersonal skills are required
- Personal/professional integrity and proven discretion in handling confidential information
- Capable of managing multiple conflicting priorities
- Availability every other weekend is required
- Fluency in English is an essential requirement
- Relevant industry experience a plus
Benefits
Comp & perks- Health/Dental/Vision Insurance Plans
- RRSP with Employer Match
- Paid Vacation and Holidays
- Paid Sick and Bereavement Leave
- Employee Assistance & Telehealth Programs
- Training & Development Programs
- Employee Referral Bonus Program
- Annual Performance Reviews
- Free parking for employees
- Accessible by public transportation