Closed listing
Clinical Research Nurse
- St. Joseph's, NL, Canada
- St Josephs, NL, Canada
Full-time
This opening has closed.
The original listing is kept below for reference.
Job details
- Job type
- Full-time
- Closing date
- Posting language
- English
- Posted
Similar jobs hiring now
Search current openingsOriginal job description
Archived listing. The details below describe a past opening.
Join the team that is revolutionizing health care – BayCare Health System
Our network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers and thousands of physicians. With the support of more than 30,000 team members, we promote a forward-thinking philosophy that’s built on a foundation of trust, dignity, respect, responsibility, and clinical excellence.
Title: Clinical Research Nurse
Facility: St. Joseph's Hospital
Responsibilities
Status: Full Time, Exempt: Yes
Shift Hours: 8:00AM - 4:30PM
Weekend Work: None
Equal Opportunity Employer Veterans/Disabled
Our network consists of 16 community-based hospitals, a long-term acute care facility, home health services, outpatient centers and thousands of physicians. With the support of more than 30,000 team members, we promote a forward-thinking philosophy that’s built on a foundation of trust, dignity, respect, responsibility, and clinical excellence.
Title: Clinical Research Nurse
Facility: St. Joseph's Hospital
Responsibilities
- Coordinates and implements research studies for assigned services under the direction of the Principal investigator in accordance with the standards of good clinical practice, federal and state regulations and institutional review board (IRB) requirements
- Ensures adherence to the study protocol and schedule of events
- Patient visit scheduling for protocol related procedures
- Screening, study recruitment, preparation of IRB reports
- Establishment and maintenance of regulatory documents
- Performing the process of informed consent and HIPPA authorization
- Clinical follow-up of study subjects
- Creation and completion of source worksheets,
- Collecting source data for electronic data capture (EDC) systems or Case Report Form (CRF) completion
- Assesses patients for trial-related and non-trial related symptoms
- Reporting of adverse events, serious adverse events, and dispensing / accountability of investigational product
- Must work independently and use sound judgment while performing job duties
- Performs duties as assigned under the scope of related certification or licensure
- Benefits (Medical, Dental, Vision)
- Paid Time Off
- Tuition Assistance
- 401K Match and additional yearly contribution
- Annual performance appraisals and team award bonus
- Family resources and wellness opportunities
- Community perks and discounts
- Required
- RN (Registered Nurse)
- Preferred
- CCRC (Clinical Research)
- Required
- Associates in Nursing
- Or - Diploma in Nursing
- Preferred
- Bachelor's in Nursing
- Required
- 2 years healthcare or management
- Preferred
- Clinical Research experience
Status: Full Time, Exempt: Yes
Shift Hours: 8:00AM - 4:30PM
Weekend Work: None
Equal Opportunity Employer Veterans/Disabled
More about this job
Responsibilities
Coordinates and implements clinical research studies, ensuring compliance with study protocols, good clinical practice, regulations, and institutional review board requirements. Manages participant scheduling, recruitment, consent, regulatory documentation, data collection, clinical follow-up, adverse event reporting, and investigational product accountability.
Requirements
An associate degree or diploma in nursing is required, and a bachelor's degree in nursing is preferred. An active Registered Nurse certification is required; two years of healthcare or management experience is required, while clinical research experience and Clinical Research Coordinator certification are preferred.
Skills
- Clinical Research Coordination
- Good Clinical Practice
- Research Protocol Compliance
- Patient Scheduling
- Patient Screening
- Study Recruitment
- Informed Consent
- HIPAA Authorization
- Institutional Review Board Reporting
- Clinical Follow-Up
- Source Data Collection
- Electronic Data Capture
- Case Report Form Completion
- Adverse Event Reporting
- Investigational Product Accountability
Benefits
- Medical Insurance
- Dental Insurance
- Vision Insurance
- Paid Time Off
- Tuition Assistance
- 401(k) Match
- Additional Yearly 401(k) Contribution
- Annual Performance Appraisals
- Team Award Bonus
- Family Resources
- Wellness Opportunities
- Community Perks and Discounts
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Science & Research
Keywords
- Registered Nurse
- Clinical Research Nurse
- Clinical Research Coordinator
- Good Clinical Practice
- Principal Investigator
- Study Protocol
- Federal Regulations
- State Regulations
- Institutional Review Board
- Patient Screening
- Study Recruitment
- Informed Consent
- HIPAA Authorization
- Regulatory Documents
- Source Worksheets
- Source Data
- Electronic Data Capture
- Case Report Forms
- Adverse Events
- Serious Adverse Events
- Investigational Product
- Clinical Follow-Up
- Nursing
- Healthcare