Nurse Practitioner

Renstar Medical Research•Ocala, FL

13h•Onsite

About The Position

Renstar Medical Research is seeking an experienced Nurse Practitioner to join our clinical research team on an as-needed (PRN) contractor basis. In this role, you will conduct physical exams and clinical assessments of research study participants under the supervision of our Principal Investigators (PIs). This position offers a flexible schedule with part-time hours; it is not a guaranteed full-time or set-hours role, and hours will fluctuate based on active study needs.

Requirements

Master's degree in Nursing (MSN) or Doctor of Nursing Practice (DNP) from an accredited program
Current, unencucumbered Florida APRN license in good standing
Current national certification (e.g., ANCC or AANP) appropriate to practice
Current BLS certification (ACLS preferred)
Prior clinical research experience preferred; willingness to work under PI oversight and study protocols required
Working knowledge of Good Clinical Practice (GCP) and FDA regulations preferred
Proficient computer skills, including Microsoft Office Suite and electronic source documentation systems
Excellent verbal and written communication skills
Ability to work independently and manage a flexible, variable schedule

Nice To Haves

ACLS preferred
Prior clinical research experience preferred
Working knowledge of Good Clinical Practice (GCP) and FDA regulations preferred

Responsibilities

Perform physical examinations and clinical assessments of research study participants under the supervision of the Principal Investigator (PI)
Evaluate participant health status, medical history, and study eligibility criteria
Conduct study visit procedures and assessments in accordance with the protocol and PI direction
Identify, document, and report adverse events and concomitant medications to the PI in a timely manner
Coordinate with research staff, PIs, and other healthcare professionals as needed
Order or review labs, diagnostics, and other assessments as delegated by the PI and permitted under Florida law
Communicate study-related findings clearly to participants, research staff, and the PI
Document all findings, assessments, and progress accurately on study-specific source documents
Review and sign study-related source documentation promptly and in accordance with study timelines
Maintain compliance with the protocol, Good Clinical Practice (GCP), and all applicable regulations