Clinical Research Registered Nurse

Jacksonville, FL - USA

Monthly Salary: Not Disclosed

Posted on: 8 days ago

Vacancies: 1 Vacancy

Job Summary

Flourish Research is looking for motivated talented creative individuals who want to learn and grow in their careers while contributing to research that changes lives!We offer an excellent comprehensive benefits package a supportive and collaborative work environment and endless growth opportunities.

We are actively hiring a Clinical Research RN at our Jacksonville (University) research site location.

The Clinical Research RN is responsible for the ethical and accurate management of Investigational Product (IP) and supplies for clinical trials under the direction of the Principal Investigator. The Research Nurse will work with Pharmacy staff and perform clinical duties requiring analysis sound judgement and a high level of knowledge of study specific protocols.

Shift: Monday - Friday 7 AM - 4 PM hours may vary
Location:4085 University Blvd. South Suite 1 Jacksonville FL 32216
Compensation: Hourly rate based on experience
Benefits: Health dental and vision insurance plans 401(k) with 4% match tuition reimbursement parental leave referral program employee assistance program life insurance disability insurance and 15 days of PTO 10 company holidays.

RESPONSIBILITIES

Maintain familiarity with FDA regulations for clinical research
Administratively and clinically manage IP for blinded and unblinded clinical trials
Adhere to company Standard Operating Procedures Good Clinical Practice and study protocols
Ensure scientific integrity of data and protect the rights safety and well-being of patients enrolled in clinicaltrials
Dispense study medication in a professional and accountable manner
Provide subjects with proper IP administration training for in-office and home dosing
Complete source documentation (Accountability logs subject source documentation etc.)
Manage IP temperatures to ensure they remain in range and report any temperature excursions accordingly
Ordering and managing IP and IP supplies
Ensure prompt reporting of events to sponsor and IRB
Assess participants condition and report any significant variations from baseline measurements to studycoordinator and Investigator
Ensure the filing and maintenance of all regulatory documents and IP related documentation
Schedule and prepare for monitoring visits
Assist monitors with accountability of used and unused IP and documentation
Maintain communication with Principal Investigator Sub Investigators Study Coordinators Assistants sponsorsand IRB

QUALIFICATIONS

Registered Nurse
At least 1 year of clinical experience
Research experience - preferred
Pleasant outgoing and mature. Good communication and time management skills. Attention to detail. Self-disciplined and motivated. Diligent and persistent.
High level of integrity and accountability
Ability to function effectively and positively in a team environment
Must have the ability to establish and maintain good working rapport with study patients physiciansinvestigators referring physicians research staff and clinic
Must exhibit accurate complete legible and timely use of communication methods
Familiar with medical terminology

Flourish Research offers an excellent comprehensive benefits package a supportive and collaborative work environment and endless growth opportunities. Apply today to learn more about how you can join us in our mission to save and improve the lives of others!

Flourish Research is where clinical trials thrive.

Flourish Research represents one of the industrys most progressive and diversified clinical trial companies with robust capabilities in the therapeutic areas of cardiology/metabolic disorders/renal CNS pulmonology and vaccines.

At Flourish Research we strive toward clinical trials and healthcare excellence means everyone deserves the best care regardless of their race color gender identity religion ethnicity physical abilities age sexual orientation or veteran status. We embrace employees customers and patients from these underrepresented groups to help make this vision a reality.

Flourish Research is driven by a diverse and inclusive community of passionate people who are committed to improving the quality of life of communities around the world. Flourish is committed to a safe work environment where all employees customers and patients are included and treated with dignity and respect.

Flourish Research strives to build an organization that attracts and leverages diversity in our staff which reflects the diversity of our local communities. We promote education acceptance and inclusion because there is beauty in diversity. The more diversity we have in our team the more unique perspectives and ideas we share and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!

It is the policy of Flourish Research not to discriminate against any applicant for employment or any employee because of age color sex disability national origin race religion or veteran status.

Required Experience:

Senior IC

Flourish Research is looking for motivated talented creative individuals who want to learn and grow in their careers while contributing to research that changes lives!We offer an excellent comprehensive benefits package a supportive and collaborative work environment and endless growth opportunities...

Maintain familiarity with FDA regulations for clinical research
Administratively and clinically manage IP for blinded and unblinded clinical trials
Adhere to company Standard Operating Procedures Good Clinical Practice and study protocols
Ensure scientific integrity of data and protect the rights safety and well-being of patients enrolled in clinicaltrials
Dispense study medication in a professional and accountable manner
Provide subjects with proper IP administration training for in-office and home dosing
Complete source documentation (Accountability logs subject source documentation etc.)
Manage IP temperatures to ensure they remain in range and report any temperature excursions accordingly
Ordering and managing IP and IP supplies
Ensure prompt reporting of events to sponsor and IRB
Assess participants condition and report any significant variations from baseline measurements to studycoordinator and Investigator
Ensure the filing and maintenance of all regulatory documents and IP related documentation
Schedule and prepare for monitoring visits
Assist monitors with accountability of used and unused IP and documentation
Maintain communication with Principal Investigator Sub Investigators Study Coordinators Assistants sponsorsand IRB

QUALIFICATIONS

Registered Nurse
At least 1 year of clinical experience
Research experience - preferred
Pleasant outgoing and mature. Good communication and time management skills. Attention to detail. Self-disciplined and motivated. Diligent and persistent.
High level of integrity and accountability
Ability to function effectively and positively in a team environment
Must have the ability to establish and maintain good working rapport with study patients physiciansinvestigators referring physicians research staff and clinic
Must exhibit accurate complete legible and timely use of communication methods
Familiar with medical terminology