Sub-Investigator / Nurse Practitioner

Sub-Investigator/ Nurse Practitioner

Miami, FL | On-site

Full-Time

Help Advance Life-Changing Clinical Research

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

Nurse Practitioner (NP) license required

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
• Patient Care
• GCP Compliance
• ICH Guidelines
• Informed Consent Process
• 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

Compensation

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

✅ Additional compensation and benefits package available

Please Note

✅ On-site in Miami, FL

✅ 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

No relocation assistance mentioned

No visa sponsorship information provided

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

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