Sub-Investigator (Nurse Practitioner)
About The Position
We are a high-performing, multispecialty clinical research site with a strong focus in gastroenterology and dermatology. In partnership with leading physician groups, we provide patients access to cutting-edge clinical trials while maintaining the highest standards of data quality, patient care, and regulatory compliance. Our site is recognized for rapid enrollment, strong retention, and operational excellence across both interventional and observational studies. We are seeking a motivated and detail-oriented Nurse Practitioner (NP) to serve as a Sub-Investigator supporting clinical trials across multiple therapeutic areas. This role is ideal for a provider interested in combining patient care with research, working alongside experienced Principal Investigators and clinical research teams. The Sub-Investigator will play a key role in subject safety, protocol adherence, and high-quality data generation while helping to drive study success and patient engagement.
Requirements
- Licensed Nurse Practitioner in the state of Florida (active and in good standing)
- Minimum 1–2 years of clinical experience required
- Strong understanding of clinical documentation and patient care standards
- Excellent communication, organization, and attention to details
- Ability to work in a fast-paced, team-oriented environment
Nice To Haves
- clinical research experience preferred
- Knowledge of Good Clinical Practice (GCP) guidelines preferred
- Experience in gastroenterology, dermatology, or internal medicine
- Prior experience as a Sub-Investigator or in a clinical research setting
- Familiarity with eSource systems (e.g., CRIO)
Responsibilities
- Perform study-related clinical assessments, including medical history, physical exams, and eligibility evaluations
- Serve as a Sub-Investigator on assigned protocols, ensuring compliance with protocol, GCP, and regulatory requirements
- Assess and document adverse events, concomitant medications, and subject safety throughout study participation
- Support informed consent discussions and ensure patient understanding of study participation
- Collaborate with study coordinators, investigators, and sponsors to ensure protocol adherence and data accuracy
- Review and sign off on study-related source documentation as delegated
- Participate in monitoring visits, audits, and sponsor interactions as needed
- Assist in recruitment efforts and patient identification in collaboration with the clinical team
- Maintain accurate, timely, and complete documentation in the eSource systems
Benefits
- Competitive compensation based on experience
- Opportunity for professional development within clinical research
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
