Clinical Research Nurse

Flourish Research•Charlotte, NC

11d•Onsite

About The Position

Flourish Research is hiring a Clinical Research Nurse to support its Charlotte, North Carolina site. The role provides comprehensive clinical, administrative, and research support within a specialized neurology practice focused on Alzheimer’s disease, dementia, and related neurodegenerative disorders. The nurse supports clinical practice and research initiatives through direct patient care, coordination of services, and clinical research responsibilities. The position is onsite, Monday through Friday on a day shift, for 40 hours per week, and is classified as non-exempt. The nurse performs IV infusions of blinded and unblinded investigational products, collects specimens, monitors participants for adverse events, and conducts clinical trial visits. The role supports participant safety and informed consent as delegated by the Principal Investigator, collaborates on study start-up, conduct, and close-out, and maintains accurate and compliant research documentation. The nurse follows FDA regulations, Good Clinical Practice, protocols, and sponsor guidelines while protecting participant confidentiality and data integrity. Work takes place onsite in a clinical office and includes daily computer use, participant care, and exposure to human bodily fluids. Local travel may be required, and occasional evening and weekend work may occur. The role requires the ability to lift 35 pounds and occasionally more, as well as the ability to drive and daily availability of an automobile.

Requirements

Graduate of an accredited nursing program; ADN or BSN preferred.
Current Registered Nurse license in good standing in the state where the site is located.
Proficiency in IV infusion and phlebotomy.
Experience providing direct patient care in a clinical setting.
Knowledge of clinical research methods and the clinical trial process, including informed consent and participant safety oversight.
Knowledge of FDA regulations and Good Clinical Practice, and ability to apply them in daily study conduct.
Strong attention to detail and documentation accuracy; working knowledge of basic statistical concepts and accurate data collection.
Strong computer skills, including electronic health records, eSource, and Office365.
Excellent organizational and time-management skills, including the ability to prioritize competing study tasks and deadlines.
Excellent oral and written communication skills, including clear communication with participants.
Ability to collaborate with investigators, coordinators, and operations.
Ability to think independently and influence when appropriate.
Ability to properly lift 35 pounds and occasionally more than 35 pounds.
Ability to drive and daily availability of an automobile.

Nice To Haves

ADN or BSN degree.
Good Clinical Practice certification.
1–2 years of clinical research experience.
Experience reviewing standard operating procedures and improving processes.

Responsibilities

Perform IV infusions of blinded and unblinded investigational products according to study protocols.
Obtain blood specimens and other biological samples from study participants using proper clinical procedures.
Monitor participants for adverse events during and after infusions and report findings according to protocols and regulatory requirements.
Serve as blinded or unblinded staff as assigned, keeping unblinded information separate and not performing blinded assessments or tasks when assigned as unblinded staff on a protocol.
Conduct clinical trial visits with participants while ensuring compliance with study protocols, ethical standards, and regulatory requirements.
Support participant safety oversight and the informed consent process as delegated by the Principal Investigator.
Collaborate with investigators, study coordinators, and clinical staff on study start-up, conduct, and close-out activities.
Communicate visit expectations clearly to participants and support a positive participant experience.
Document, manage, and maintain accurate, complete, timely, and protocol-compliant research records and source documentation.
Follow FDA regulations, Good Clinical Practice, and sponsor guidelines; support required reporting and documentation activities.
Maintain the confidentiality and integrity of study data and participant information.
Participate in training and maintain current knowledge of clinical trial procedures and safety standards.
Represent Flourish Research professionally and courteously when interacting with staff, clients, and vendors.
Perform additional duties as assigned by management.