Nurse Practitioner/Sub-Investigator

Civia Health; Independence (MO); On-site; USD 80,000 - 100,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

Generous PTO and paid holidays

Flexible scheduling options

Professional development support

Job summary

Civia Health is looking for a dedicated Nurse Practitioner or Physician's Assistant to join their team in Independence, Missouri. The role involves conducting study visits, ensuring compliance, and engaging with participants while maintaining high-quality documentation.

Ideal candidates will have an active license and at least 2 years of clinical research experience, particularly in metabolic or endocrine research. Competitive compensation, medical benefits, and flexible scheduling options are provided.

Qualifications

• Must have an active, unrestricted Nurse Practitioner or Physician's Assistant license.
• Requires 2+ years of clinical research experience, preferably in Phase 2-4 trials.
• Familiarity with GLP-1 therapies or metabolic/endocrine research is highly desired.

Responsibilities

• Conduct study visits, including medical assessments and procedures.
• Partner with investigators to ensure quality and regulatory compliance.
• Engage participants empathetically, addressing their questions.

Skills

Clinical judgment

Attention to detail

Communication skills

Collaboration

Education

Active Nurse Practitioner or Physician's Assistant license

2+ years of clinical research experience

Job description

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