Nurse Practitioner

Key Responsibilities

• Perform protocol-specified physical exams, medical histories, and study visits
• Assess eligibility criteria and co-sign source documentation with the PI
• Order and interpret labs / diagnostics per study requirements
• Counsel participants on study procedures, investigational products, and adverse-event reporting
• Manage and document AEs/SAEs, escalating to PI and sponsor as required
• Maintain GCP-compliant source notes and electronic medical records
• Support recruitment and retention initiatives (community outreach, phone screenings, etc.)
• Participate in investigator meetings, SIVs, monitoring visits, and audits
• Contribute to continuous improvement of site SOPs and quality metrics

Minimum Qualifications

• Currently, unrestricted GA license as NP or PA-C
• National certification (AANP/ANCC or NCCPA)
• BLS (ACLS preferred)
• 2+ years of direct patient-care experience (family practice, internal medicine, ER/urgent care, or wound care a plus)
• Familiarity with—or strong interest in—clinical research and FDA/GCP guidelines
• EMR proficiency and solid documentation skills
• Excellent communication and interpersonal abilities

Preferred Qualifications

• Prior experience as a Sub-Investigator or treating provider in clinical trials
• Spanish-speaking (or other community language)
• Phlebotomy and IV skills

Compensation & Perks

• Competitive hourly rate commensurate with experience
• Flexible, family-friendly schedule
• Opportunity to convert to full-time as site expands

Note

The work schedule for this role is as follows:

• Monday: Afternoon shift
• Tuesday – Thursday: Full-day, on-site (9:00 AM – 5:00 PM)