Clinical Research Nurse Practitioner

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

• Ensure the safety of study participants, and maintain communication with their families/caregivers and clinicians.
• Provide clinical and administrative medical support and oversight for research clinical trials based on scope of practice; obtain complete study participant history, conduct physical exams, review medical charts, assess findings, prescribe and re-fill medication, and perform designated procedures according to written protocols.
• Collaborate with clinical staff, researchers, outside vendors, and other staff to administer treatment and study protocols.
• Assess, grade, and document adverse events; apply triage and judgment to determine course of action.
• Oversee and as needed, administer medications and treatments per study protocol and scope of practice.
• Comply with institutional policies, standard operating procedures, and guidelines; prepare and submit documentation as required by the study protocol and study sponsor; interpret complex protocols and regulatory requirements.
• Coordinate and collaborate with principal investigator to review study protocol; assess and analyze feasibility, budget projections, and staffing needs.
• Supervise and train non- clinical and clinical staff/students, as needed.
• Identify, recruit, and enroll study participants, as well as maintain study participant records; determine study participant criteria.
• Support sponsor investigator research with investigational new drug/investigational device exemption applications.

• Bachelor's degree in nursing or equivalent, and five years of experience in nursing, with at least two years in a research setting.
• Excellent Verbal and written communications
• Ability to implement good clinical practices in all interactions with study participants, their families, and colleagues.
• Ability to implement study protocols with minimal supervision.