What are the responsibilities and job description for the Sub-Investigator / Nurse Practitioner position at BioTalent?
🚀 Sub-Investigator
📍 Rogers, AR | 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: $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
🚫 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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Salary : $150,000 - $175,000