Sub-Investigator / Nurse Practitioner

BioTalent; Rogers (AR); On-site; USD 150,000 - 175,000; Full time

Job summary

BioTalent is seeking a Nurse Practitioner to join our clinical research team as a Sub-Investigator, supporting Phase I–IV studies across neuroscience, psychiatry, neurology, acute pain, and metabolic disorders.

You will conduct visits, monitor safety, ensure GCP/ICH compliance, manage informed consent, and collaborate with sponsors, IRBs, and site staff. On-site in Rogers, AR with potential travel.

Qualifications

• Experience as a Sub-Investigator in industry-sponsored trials preferred.
• Understanding of GCP, ICH guidelines, and regulatory requirements.
• Active NP license is required to practice as a medical provider in studies.

Responsibilities

• Serve as the medical provider supporting the Principal Investigator in oversight of clinical trials.
• Conduct study visits, medical evaluations, and ongoing assessments for research participants.
• Ensure compliance with study protocols, GCP, ICH guidelines, and regulatory requirements.
• Monitor participant safety, evaluate adverse events, and provide medical care as needed.
• Lead and oversee the informed consent process to protect participant rights and welfare.
• Collaborate with sponsors, monitors, IRBs, physicians, and research staff throughout the study lifecycle.
• Review and maintain accurate clinical documentation, source records, and study data.
• Support patient recruitment, study enrollment, site operations, audits, and overall trial execution from a clinical and regulatory perspective.

Skills

Clinical Research

Medical Terminology

GCP Compliance

ICH Guidelines

Regulatory Compliance

IRB Processes

Subject Recruitment

Clinical Documentation

Sponsor & Monitor Interactions

Clinical Operations

Communication & Presentation

Relationship Building

Education

Nurse Practitioner license

Tools

Microsoft Office

Clinical Research Systems

Job description

Great opportunity for Nurse Practitioners interested in clinical research and patient-focused studies

Are you passionate about clinical research, patient care, and advancing innovative therapies? We're looking for a Sub-Investigator to join a growing clinical research team supporting Phase I-IV studies across a variety of therapeutic areas, including neuroscience, psychiatry, neurology, acute pain, and metabolic disorders.

If you thrive in a fast-paced clinical environment and want to contribute to cutting-edge research that helps bring new therapies to patients, this could be your next opportunity.

What You'll Do

• Serve as the medical provider supporting the Principal Investigator in the oversight of clinical trials
• Conduct study visits, medical evaluations, and ongoing assessments for research participants
• Ensure compliance with study protocols, GCP, ICH guidelines, and regulatory requirements
• Monitor participant safety, evaluate adverse events, and provide appropriate medical care when needed
• Lead and oversee the informed consent process to protect participant rights and welfare
• Collaborate with sponsors, study monitors, IRBs, physicians, and research staff throughout the study lifecycle
• Review and maintain accurate clinical documentation, source records, and study-related data
• Support patient recruitment, study enrollment, site operations, audits, and overall trial execution from a clinical and regulatory perspective

What We're Looking For

• Experience as a Sub-Investigator in industry-sponsored clinical trials preferred
• Understanding of Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and regulatory requirements
• Skills and knowledge in:
• Clinical Research
• Medical Terminology
• GCP Compliance
• ICH Guidelines
• Regulatory Compliance
• IRB Processes
• Subject Recruitment and Retention
• Clinical Documentation
• Sponsor and Monitor Interactions
• Clinical Operations
• Communication and Presentation Skills
• Negotiation and Relationship Building
• Microsoft Office (Word, Excel) and Clinical Research Systems

Base Salary: $150,000 - $175,000 annually, depending on experience and qualifications.

Additional compensation and benefits package available

Please Note

• On-site in Rogers, AR
• Full-time clinical research position
• Opportunity to support Phase I-IV clinical trials
• Ability to travel overnight as needed
• Must maintain an active NP license