Clinical Research Nurse - 259360
- Cambridge, ON, Canada
$45 to $58.98 USD / hour · Full-time
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Job details
- Pay
- $45 to $58.98 USD / hour
- Job type
- Full-time
- Apply by
- Posting language
- English
- Posted
Original job description
This Full time on site position offers great opportunities for career growth. Our client seeks an EXPERIENCED FULL-TIME, IN-CLINIC RN Clinical Research Coordinator with research-based nursing experience in-person Phase III Clinical Trials.
Ability to think, problem solve, prioritize, demonstrate proficiency in computer communications, self-directed, independent work. Demonstrated excellence in communication, organization, & collaboration.
The nurse will coordinate clinical trials.
Job details:
- Conducting clinical trials according to study protocol
- Screening patients for inclusion and exclusion criteria
- Patient visits
- Data collection
- Entering data into electronic case report forms
- Collecting vital signs
- Performing ECGs
- Drawing blood work
- Lab specimen preparation and shipment
- Manage adverse and serious adverse events
- Travel to investigator meetings
Requirements:
- Current RN status, in good standing with the College of Nurses of Ontario and be able to work in Ontario
- Only applicants currently residing in Canada, with a valid licence to work in Ontario will be considered
- Bachelor of Science in Nursing (BScN) or equivalent
- Cardiology, ICU, ER or office-based experience
- More than 2 years
- Current Valid Ontario RN License
- Ability to think critically, solve situations based on protocols and algorithms
- Work independently
- Multitask
- Current Passport
- Ability to travel to the US for investigator meetings
- Excellent Venipuncture skills
- Excellent Computer skills
- Excellent interpersonal skills
- Current Covid vaccinations
Pay & Benefits:
- Matching ONA Pay grid
- Benefits
- Pension Plan not available currently
- Job Type: Full-time, Permanent
- Pay: $45.00–$58.98 per hour
- Benefits: Dental care, Extended health care, Life insurance
Experience:
- Working as an RN/RPN in Ontario: 2 years (required)
Licence/Certification:
- Current RPN/RN Licence and work experience in Ontario (required)
More about this job
Responsibilities
Coordinate Phase III clinical trials in accordance with study protocols, including screening patients, conducting visits, collecting data, and entering information into electronic case report forms. Perform clinical procedures and laboratory tasks, manage adverse events, and travel to investigator meetings.
Requirements
Requires a current Ontario RN licence in good standing, a BScN or equivalent, and more than two years of relevant nursing experience, such as in cardiology, ICU, emergency, or office-based care. Candidates must be able to work independently, think critically, communicate and collaborate effectively, demonstrate strong venipuncture and computer skills, hold a current passport, and be able to travel to the United States.
Skills
- Clinical Trial Coordination
- Clinical Research Nursing
- Protocol Compliance
- Patient Screening
- Patient Visits
- Data Collection
- Electronic Case Report Forms
- Vital Signs Measurement
- Electrocardiograms
- Venipuncture
- Blood Draws
- Laboratory Specimen Preparation and Shipment
- Adverse Event Management
- Critical Thinking
- Problem Solving
- Computer Skills
Benefits
- Dental Care
- Extended Health Care
- Life Insurance
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Science & Research
Keywords
- Registered Nurse
- Clinical Research Coordinator
- Clinical Trials
- Phase III
- Study Protocol
- Patient Screening
- Inclusion and Exclusion Criteria
- Patient Visits
- Data Collection
- Electronic Case Report Forms
- Vital Signs
- Electrocardiograms
- Venipuncture
- Blood Draws
- Laboratory Specimens
- Adverse Events
- Serious Adverse Events
- Cardiology
- Intensive Care Unit
- Emergency Room
- Ontario RN Licence
- BScN
- Investigator Meetings
- Clinical Research Nursing