Nurse Practitioner/Sub-Investigator

Job Type: Full-time, on-site Reports to: Director, Site Management What You’ll Do Conduct study visits including medical assessments, physical exams, and protocol-specific procedures. Partner with principal investigators and research staff to ensure quality, safety, and regulatory compliance. Engage participants with empathy—providing clear education, answering questions, and ensuring comfort throughout the trial process. Identify, document, and report adverse events per protocol and regulatory standards. Maintain accurate, timely, and high-quality documentation in source records and EDC systems. Contribute to continuous improvement of workflows and study execution with a team-first mindset. Occasional travel may be required for audits, site visits, or team meetings. What You Bring Active, unrestricted Nurse Practitioner license or Physician's Assistant license. 2+ years of clinical research experience (Phase 2–4 trials preferred). Experience with GLP-1 therapies or metabolic/endocrine research highly preferred. Strong knowledge of GCP/ICH guidelines; certification is a plus. Excellent clinical judgment, attention to detail, and communication skills. A collaborative spirit and commitment to doing what’s best for the patient and the team. What We Offer Competitive compensation Medical, dental, and vision insurance Generous PTO and paid holidays Flexible scheduling options Professional development and continuing education support A mission-driven team that values respect, inclusion, and innovation #J-18808-Ljbffr