Sub-Investigator/Nurse Practitioner

Green Life Science; Arkansas; On-site; USD 95,000 - 170,000; Full time

Job summary

Green Life Science, a leading U.S. clinical research organization, seeks an experienced Nurse Practitioner to join as Sub-Investigator. This role provides medical oversight of trial participants and collaboration with PIs, sponsors and research teams.

You will conduct clinical assessments, consent processes, safety reporting, and support successful trial delivery; travel for investigator meetings may be needed.

Qualifications

• Clinical research experience required.
• Strong knowledge of GCP, ICH, and FDA regulations.
• Experience conducting clinical assessments and patient visits.
• Understanding of protocols, informed consent, and safety reporting.
• Industry-sponsored clinical trials experience preferred.
• Phase I–IV experience highly desirable.
• CNS / Psychiatry / Neurology / Pain experience a plus.
• Willingness to travel occasionally for investigator meetings.

Responsibilities

• Medical oversight of trial participants.
• Protocol review and safety assessments.
• Obtain informed consent and monitor safety reporting.
• Support the PI with successful delivery of trials.

Skills

Clinical research

GCP/ICH/FDA

Patient visits

Informed consent

Safety reporting

Phase I–IV experience

Neurology experience

Travel willingness

Job description

I’m working with a leading U.S. clinical research organisation looking for an experienced Nurse Practitioner to join as a Sub-Investigator.

A great opportunity for an NP looking to take on greater medical responsibility within clinical research and work closely with experienced PIs, sponsors and research teams.

What they’re looking for:

• Clinical research experience
• Strong knowledge of GCP / ICH / FDA regulations
• Experience conducting clinical assessments and patient visits
• Understanding of protocols, informed consent & safety reporting
• Industry-sponsored clinical trial experience preferred
• Phase I–IV experience highly desirable
• CNS / Psychiatry / Neurology / Pain experience a plus
• Ability to travel occasionally for investigator meetings

What you'll be doing:

Medical oversight of trial participants, protocol review, safety assessments, informed consent, sponsor/monitor interaction and supporting the PI with the successful delivery of clinical trials.