Actalent
Research Nurse Neuro
Actalent, Orlando, Florida, us, 32885
Neurology Registered Nurse
Qualifications
Ideally 2 years of Neurology nursing experience
Associate degree in Nursing
Active State of Florida Registered Nurse license
BLS certification
Ability to perform clinical tasks, including assisting physicians and CRNs with minor procedures and other study requirements within the scope of practice
Ability to acclimate and integrate into various clinical settings as needed per protocol
Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion, and administration of investigational drugs
Clinical Research Nurse Coordinator
The Neurology Registered Nurse Coordinator will work under limited supervision to plan, coordinate, evaluate, and perform nursing care for research participants
The Neurology Registered Nurse Coordinator will collect data for assigned research projects, following study-specific protocol guidelines, and will communicate with Principal Investigators (PI), Sub-Investigators (Sub-I), Clinical Research Lead, and clinical research support staff
Deliver safe care and demonstrate regard for the dignity and respect of all participants
Maintain clinical competencies including physical assessment, phlebotomy, and IV insertion
Practice the principles of Universal Precautions and adhere to HIPAA regulations
Maintain a clean and prepared clinical space, performing set-up and turnover procedures in all clinical areas as per SOPs
Participate in internal and/or external training programs to maintain licensure
Utilize positive interpersonal communication skills, effectively communicating with healthcare team members, patients, investigators, sponsors of research, and administration
Review all elements of the current institutional IRB-approved informed consent document with study candidates and/or their legal representatives, ensuring patient advocacy and informed consent as an ongoing process
Manage multiple clinical trial protocols, coordinate their execution and follow-up, and ensure accurate, legible, and timely documentation
Manage records, study medication, and test articles in a confidential and secure manner
Promote PI oversight by advising the PI, sub-investigator(s), Supervisor, and/or Clinical Operations Manager of deviations in conduct, patient status, and issues relevant to the integrity of the trial and/or safety of research subjects
Coordinate the work of support staff, laboratory technicians, and assistants to ensure efficient, timely, and high-quality results and adherence to research protocols
Pay and Benefits
The pay range for this position is $74880.00 - $98000.00
Benefits from Day One
Paid Days Off from Day One
Career Development
Whole Person Wellbeing Resources
Mental Health Resources and Support
Pet Insurance*
Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense)
Workplace Type
This is a fully onsite position in Orlando,FL.
Application Deadline
This position will be accepting applications until Jan 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.
Qualifications
Ideally 2 years of Neurology nursing experience
Associate degree in Nursing
Active State of Florida Registered Nurse license
BLS certification
Ability to perform clinical tasks, including assisting physicians and CRNs with minor procedures and other study requirements within the scope of practice
Ability to acclimate and integrate into various clinical settings as needed per protocol
Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion, and administration of investigational drugs
Clinical Research Nurse Coordinator
The Neurology Registered Nurse Coordinator will work under limited supervision to plan, coordinate, evaluate, and perform nursing care for research participants
The Neurology Registered Nurse Coordinator will collect data for assigned research projects, following study-specific protocol guidelines, and will communicate with Principal Investigators (PI), Sub-Investigators (Sub-I), Clinical Research Lead, and clinical research support staff
Deliver safe care and demonstrate regard for the dignity and respect of all participants
Maintain clinical competencies including physical assessment, phlebotomy, and IV insertion
Practice the principles of Universal Precautions and adhere to HIPAA regulations
Maintain a clean and prepared clinical space, performing set-up and turnover procedures in all clinical areas as per SOPs
Participate in internal and/or external training programs to maintain licensure
Utilize positive interpersonal communication skills, effectively communicating with healthcare team members, patients, investigators, sponsors of research, and administration
Review all elements of the current institutional IRB-approved informed consent document with study candidates and/or their legal representatives, ensuring patient advocacy and informed consent as an ongoing process
Manage multiple clinical trial protocols, coordinate their execution and follow-up, and ensure accurate, legible, and timely documentation
Manage records, study medication, and test articles in a confidential and secure manner
Promote PI oversight by advising the PI, sub-investigator(s), Supervisor, and/or Clinical Operations Manager of deviations in conduct, patient status, and issues relevant to the integrity of the trial and/or safety of research subjects
Coordinate the work of support staff, laboratory technicians, and assistants to ensure efficient, timely, and high-quality results and adherence to research protocols
Pay and Benefits
The pay range for this position is $74880.00 - $98000.00
Benefits from Day One
Paid Days Off from Day One
Career Development
Whole Person Wellbeing Resources
Mental Health Resources and Support
Pet Insurance*
Debt-free Education* (Certifications and Degrees without out-of-pocket tuition expense)
Workplace Type
This is a fully onsite position in Orlando,FL.
Application Deadline
This position will be accepting applications until Jan 10, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.