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 - Medical, dental, and vision insurance
- Generous PTO and paid holidays
- Flexible scheduling options
- Professional development and continuing education support
If you're ready to be part of something meaningful-and work with people who care deeply about doing good work-apply today by submitting your resume and cover letter to the link above. We're excited to learn more about you!
