Sub l /Nurse Practitioner

Evolution Research Group•Little Rock, AR

21d

About The Position

The Sub-Investigator serves as a secondary clinician responsible for clinical and medical oversight at the research site, acting on behalf of the Principal Investigator as needed. This role supports the execution of clinical trials in compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements while ensuring subject safety and data integrity.

Requirements

APRN with active medical license required
Knowledge of FDA regulations, IRB requirements, and GCP standards
Strong attention to detail and commitment to subject safety
Ability to work collaboratively in a clinical research environment

Nice To Haves

Experience as a Sub-Investigator in industry-sponsored clinical trials preferred

Responsibilities

Conduct subject medical visits and oversee clinical aspects of active studies
Support patient recruitment and enrollment efforts
Ensure protocol adherence, informed consent compliance, and subject safety
Evaluate and report adverse events per protocol and regulatory guidelines
Collaborate with the Principal Investigator, study monitors, IRB, and site staff
Participate in investigator meetings, monitoring visits, and audits
Ensure accuracy, completeness, and timeliness of clinical trial data and documentation
Oversee proper use and storage of investigational products
Assist with study feasibility review and selection
Communicate effectively with sponsors, research teams, and subjects
Maintain active medical licensure and current CV
Sign required regulatory documents (FDA 1572, protocols, sponsor agreements)
Ensure IRB approvals are obtained and maintained
Uphold subject rights, welfare, and confidentiality
Ensure compliance with GCP, ICH guidelines, and SOPs