Sub-Investigator / Nurse Practitioner

BioTalent; New York (NY); On-site; USD 100,000 - 150,000; Full time

Job summary

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

You will oversee the medical provider role, conduct visits, ensure regulatory compliance, monitor safety, and guide informed consent processes while collaborating with sponsors and IRBs.

Qualifications

• Active Nurse Practitioner license required.
• Experience as Sub-Investigator in industry-sponsored trials preferred.
• Solid understanding of GCP, ICH guidelines, and regulatory requirements.

Responsibilities

• Support Principal Investigator in overseeing clinical trials.
• Conduct study visits, medical evaluations, and ongoing assessments.
• Ensure compliance with study protocols, GCP and ICH guidelines.

Skills

Clinical Research

GCP Compliance

ICH Guidelines

Regulatory Compliance

IRB Processes

Communication Skills

Microsoft Office

Clinical Documentation

Sponsor and Monitor Interactions

Presentation Skills

Tools

Microsoft Office (Word, Excel)

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: $100,000 - $150,000 annually, depending on experience and qualifications.

Additional compensation and benefits package available

Please Note

• 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

If this sounds like you, or someone in your network, I'd love to connect!

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