Sub-Investigator: Austin, TX; Shelby Township, MI; Kansas City, MO; St. Louis, MO; Goodlettsville, TN; La Vergne, TN; Memphis, TN and Raleigh, NC

Civia Health•Short Hills, NJ

About The Position

The Nurse Practitioner/PA/Sub-Investigator conducts clinical research study visits, including medical assessments, physical examinations, and protocol-specific procedures. The role partners with principal investigators and research staff to support study quality, participant safety, and regulatory compliance. It also involves educating and supporting participants, documenting and reporting adverse events, and maintaining accurate records in source documentation and electronic data capture (EDC) systems. The position contributes to workflow and study-execution improvements in a collaborative, team-first environment. Occasional travel may be required for audits, site visits, or team meetings. The position is offered across locations in Austin, Texas; Shelby Township, Michigan; Kansas City and St. Louis, Missouri; Goodlettsville, La Vergne, and Memphis, Tennessee; and Raleigh, North Carolina. The employer offers competitive compensation, medical, dental, and vision insurance, generous paid time off and paid holidays, flexible scheduling options, and professional development and continuing education support. The posting describes a mission-driven culture centered on health equity, respect, inclusion, innovation, collaboration, transparency, and employee growth.

Requirements

Hold an active, unrestricted Nurse Practitioner license or Physician Assistant license.
Have at least 2 years of clinical research experience; Phase 2–4 trials are preferred.
Demonstrate strong knowledge of GCP/ICH guidelines.
Bring excellent clinical judgment, attention to detail, and communication skills.
Have a collaborative spirit and commitment to what is best for patients and the team.

Nice To Haves

Experience with GLP-1 therapies or metabolic/endocrine research is highly preferred.
GCP/ICH certification is a plus.

Responsibilities

Conduct study visits, including medical assessments, physical exams, and protocol-specific procedures.
Partner with principal investigators and research staff to ensure study quality, participant safety, and regulatory compliance.
Provide participants with clear education, answer questions, and support their comfort throughout the trial process.
Identify, document, and report adverse events according to protocol and regulatory standards.
Maintain accurate, timely, high-quality documentation in source records and EDC systems.
Contribute to continuous improvement of workflows and study execution with a team-first mindset.
Occasionally travel for audits, site visits, or team meetings.