Clinical Research Associate RN (Oncology)
Fort Lauderdale, FLFull-time
Behavioral Health Market Context
Apply Nowvia Talents By Vaia
Benefits
Dental CoveragePaid Time OffHealth Insurance
Job Description
uch as: subject recruitment, confirming eligibility, obtaining informed consent, completing case report forms, data clarification, IRB preparations, chart abstraction, hosting monitor visits, and organizing site initiation visits. The person will lead and manage the project from a clinical research perspective, with full understanding of GCP and regulations, ensuring compliance with policies from IRB, FDA, ICH, and other sources. Experience with cardiology clinical trials and industry-sponsored studies is preferred.
Purpose: This role involves conducting oncology clinical research activities. The candidate should have industry-sponsored clinical trial experience and be knowledgeable about GCP and regulations. They will be responsible for ensuring adherence to all relevant policies and maintaining up-to-date knowledge from IRB, FDA, ICH, GCP, or other sources.
• FL RN License Required
• On-Site
What you will do:
• Assist in recruiting study participants.
• Screen patient charts for eligibility.
• Evaluate protocol patients' charts and advise investigators on tests needed.
• Coordinate collection of laboratory testing (blood, bone marrow, urine, etc.) and extract data from source documents.
• Assist investigators in evaluating, documenting, and reporting adverse events and safety data.
• Conduct telephone screenings and educate patients and families about clinical trials.
• Obtain informed consent ensuring patient understanding.
• Maintain accurate regulatory documentation, including IRB and FDA approvals and reports.
• Participate in site initiation, monitoring, and close-out visits.
Minimum Qualifications:
Education:
• Graduate of an accredited nursing school; BSN preferred.
Licensure/Certification:
• FL RN license
Position Highlights and Benefits:
• Comprehensive benefits including medical, dental, vision, paid time off, 403B, and education assistance.
• Serving as a compassionate and transforming healing presence within our communities.
• Guiding behaviors: supporting each other, open and respectful communication, full presence, accountability, trust, and positive intent.
• Ministry/Facility Information:
• Holy Cross Hospital, Fort Lauderdale, FL, a full-service, non-profit Catholic hospital sponsored by the Sisters of Mercy, part of Trinity Health.
• Committed to holistic, person-centered care.
• The only Catholic hospital in Broward and Palm Beach counties, part of a large national health system serving 21 states with nearly 2.8 million visits annually.
• Benefits start from the first day of work.
• Retirement savings with employer matching.
Legal Info:
We are an Equal Opportunity Employer and do not discriminate based on race, color, sex, age, national origin, religion, sexual orientation, gender identity, veteran status, disability, or other protected classes.
Our Commitment:
Rooted in our Mission and Core Values, we honor the dignity of every person and value the diverse perspectives and talents of our colleagues. We embrace differences to grow stronger and provide compassionate, person-centered care. We are committed to equal opportunity employment, ensuring consideration for all qualified applicants regardless of protected statuses.
#J-18808-Ljbffr
Purpose: This role involves conducting oncology clinical research activities. The candidate should have industry-sponsored clinical trial experience and be knowledgeable about GCP and regulations. They will be responsible for ensuring adherence to all relevant policies and maintaining up-to-date knowledge from IRB, FDA, ICH, GCP, or other sources.
• FL RN License Required
• On-Site
What you will do:
• Assist in recruiting study participants.
• Screen patient charts for eligibility.
• Evaluate protocol patients' charts and advise investigators on tests needed.
• Coordinate collection of laboratory testing (blood, bone marrow, urine, etc.) and extract data from source documents.
• Assist investigators in evaluating, documenting, and reporting adverse events and safety data.
• Conduct telephone screenings and educate patients and families about clinical trials.
• Obtain informed consent ensuring patient understanding.
• Maintain accurate regulatory documentation, including IRB and FDA approvals and reports.
• Participate in site initiation, monitoring, and close-out visits.
Minimum Qualifications:
Education:
• Graduate of an accredited nursing school; BSN preferred.
Licensure/Certification:
• FL RN license
Position Highlights and Benefits:
• Comprehensive benefits including medical, dental, vision, paid time off, 403B, and education assistance.
• Serving as a compassionate and transforming healing presence within our communities.
• Guiding behaviors: supporting each other, open and respectful communication, full presence, accountability, trust, and positive intent.
• Ministry/Facility Information:
• Holy Cross Hospital, Fort Lauderdale, FL, a full-service, non-profit Catholic hospital sponsored by the Sisters of Mercy, part of Trinity Health.
• Committed to holistic, person-centered care.
• The only Catholic hospital in Broward and Palm Beach counties, part of a large national health system serving 21 states with nearly 2.8 million visits annually.
• Benefits start from the first day of work.
• Retirement savings with employer matching.
Legal Info:
We are an Equal Opportunity Employer and do not discriminate based on race, color, sex, age, national origin, religion, sexual orientation, gender identity, veteran status, disability, or other protected classes.
Our Commitment:
Rooted in our Mission and Core Values, we honor the dignity of every person and value the diverse perspectives and talents of our colleagues. We embrace differences to grow stronger and provide compassionate, person-centered care. We are committed to equal opportunity employment, ensuring consideration for all qualified applicants regardless of protected statuses.
#J-18808-Ljbffr
Qualifications
- •The candidate should have industry-sponsored clinical trial experience and be knowledgeable about GCP and regulations
- •FL RN license
Benefits
- •Comprehensive benefits including medical, dental, vision, paid time off, 403B, and education assistance
- •Serving as a compassionate and transforming healing presence within our communities
- •Benefits start from the first day of work
- •Retirement savings with employer matching
Responsibilities
- •This person will be responsible for conducting multiple clinical research activities
- •The ideal candidate will have experience with industry-sponsored clinical trials and/or project management for investigator-initiated projects
- •They should be able to work independently within the scope of clinical research protocols and participate in activities such as: subject recruitment, confirming eligibility, obtaining informed consent, completing case report forms, data clarification, IRB preparations, chart abstraction, hosting monitor visits, and organizing site initiation visits
- •The person will lead and manage the project from a clinical research perspective, with full understanding of GCP and regulations, ensuring compliance with policies from IRB, FDA, ICH, and other sources
- •Purpose: This role involves conducting oncology clinical research activities
- •They will be responsible for ensuring adherence to all relevant policies and maintaining up-to-date knowledge from IRB, FDA, ICH, GCP, or other sources
- •FL RN License Required
- •Assist in recruiting study participants
- •Screen patient charts for eligibility
- •Evaluate protocol patients' charts and advise investigators on tests needed
- •Coordinate collection of laboratory testing (blood, bone marrow, urine, etc.) and extract data from source documents
- •Assist investigators in evaluating, documenting, and reporting adverse events and safety data
- •Conduct telephone screenings and educate patients and families about clinical trials
- •Obtain informed consent ensuring patient understanding
- •Maintain accurate regulatory documentation, including IRB and FDA approvals and reports
- •Participate in site initiation, monitoring, and close-out visits
- •Guiding behaviors: supporting each other, open and respectful communication, full presence, accountability, trust, and positive intent
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