Sub-Investigator/ Nurse Practitioner
Miami, FL | On-site
Full-Time
If you are interested in applying for this job, please make sure you meet the following requirements as listed below.
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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Sub-Investigator / Nurse Practitioner in miami at Unknown Company
This position is listed as full time and onsite.