Clinical Research Nurse

Flourish Research is where clinical trials thrive.

Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In 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 is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. 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.

WESEEYOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!

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 Nurse to support our Charlotte, NC site.

Shift: Monday-Friday day shift (40 hours per week)

Location:

Onsite, Charlotte, NC

FLSA Classification:
Non-Exempt

• Infusion and specimen collection
• A. Perform IV infusion of blinded and unblinded investigational products according to study protocols.
• B. Obtain blood specimens and other biological samples from study participants following proper clinical procedures.
• C. Monitor participants for adverse events during and after infusion and report findings per protocol and regulatory requirements.
• D. Serve as blinded or unblinded staff as assigned per protocol. When assigned as unblinded staff on a protocol, keep unblinded information separate and do not perform blinded assessments or blinded study tasks on that protocol.
• Study conduct
• E. Conduct clinical trial visits by working directly with study participants, ensuring compliance with study protocols, ethical standards and regulatory requirements.
• F. Support participant safety oversight and the informed consent process as delegated by the Principal Investigator.
• G. Collaborate with investigators, study coordinators and other clinical staff to support study start-up, conduct and close-out activities.
• H. Communicate clearly with participants about visit expectations and support a positive participant experience.
• Documentation and compliance
• I. Document, manage and maintain research records and source documentation that are accurate, complete, timely and protocol-compliant.
• J. Follow FDA regulations, Good Clinical Practice (GCP) and sponsor guidelines, and support required reporting and documentation activities.
• K. Maintain the confidentiality and integrity of study data and participant information.
• L. Participate in training and maintain current knowledge of clinical trial procedures and safety standards.
• General
• M. Represent Flourish Research in a professional and courteous manner (verbal, written and in appearance) when interacting with all staff, clients and vendors.
• N. Additional duties as assigned by management.

• A. Work is performed on-site in a clinical office setting.
• B. Local travel may be required as needed.
• C. Daily computer use.
• D. Exposure to human bodily fluids.
• E. Participant/patient care.
• F. Occasional evening and weekend work schedules.
• G. Ability to properly lift thirty-five…