Clinical Research Nurse - 259360

Job summary

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.

Job details

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)

What you’ll do

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.

Benefits

• Dental Care
• Extended Health Care
• Life Insurance

Listed skills

• Problem solving · Preferred
• Critical Thinking · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• 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

Job areas

• Healthcare
• Science & Research