Clinical Research Nurse

Maxonic maintains a close and long-term relationship with our direct client. In support of their needs, we are looking for a

• Support the safety of study participants and maintain communication with their families/caregivers and clinicians.
• Provide clinical and administrative nursing support for research clinical trials based on scope of practice. Collaborate with clinical staff, researchers, outside vendors, and other staff to administer treatment and study protocols. May coordinate multi-site studies.
• Conduct study participant evaluations according to the study protocol, assess adverse events, and apply triage and judgment to determine course of action.
• Administer medications and treatments per study protocol for out study participant research participants. May collect, process, and ship lab specimens.
• Comply with institutional policies, standard operating procedures, and guidelines, and prepare and submit documentation as required by the study protocol, study sponsor, and regulatory authorities.
• Manage essential regulatory documents and handle confidential information (verbal and written) with tact and diplomacy, adhering to all HIPAA guidelines.
• Supervise research staff, coordinating staffing or scheduling assignments as needed.
• Participate in budget preparation and billing reconciliation.
• Identify, recruit, and enroll study participants. Participate in the informed consent process.
• Participate and host monitor visits.
• Assist sponsor investigator research with Investigational New Drug/Investigational Device Exemption applications.