Clinical Sub-Investigator (PA/NP) — Research Trials

Dm Clinical Research Group; Sugar Land (TX); On-site; USD 85,000 - 120,000; Full time

Job summary

Dm Clinical Research Group is seeking a Sub-Investigator (Physician Assistant or Nurse Practitioner) to ensure protocol adherence, protect subject welfare, and direct study conduct under the Principal Investigator. The role requires current nursing licensure and clinical research experience, with responsibilities spanning safety monitoring, procedures, data integrity, and regulatory compliance.

You will manage the clinical staff at the site, assist in trial-related decisions, and participate in

Qualifications

• Bachelor's or Master's in Nursing and active nursing licensure.
• Current nursing licensure in good standing (PA or NP).
• Clinical research experience preferred.

Responsibilities

• Ensure adherence to protocol requirements and protect subjects' rights.
• Direct the conduct of research per federal/state regulations and guidance.
• Complete DMCR-required training including GCP and IATA.
• Maintain up-to-date licensure and CV.
• Supervise clinical staff activities at the site.
• Perform clinical-related procedures and trial-related decisions as delegated by PI.
• Conduct safety assessments and monitor trial participation (exams, phlebotomy, lab work).
• Document study procedures and events; attend investigator meetings as needed.

Skills

Clinical research knowledge

Communication skills

Diagnostic skills

Ethical and legal healthcarePrinciples

English proficiency (verbal & written)

Bilingual English/Spanish (preferred)

Education

Bachelor's or Master's in Nursing

Job description

Dm Clinical Research Group is seeking a Sub-Investigator (Physician Assistant or Nurse Practitioner) to ensure protocol adherence, protect subject welfare, and direct study conduct under the Principal Investigator. The role requires current nursing licensure and clinical research experience, with responsibilities spanning safety monitoring, procedures, data integrity, and regulatory compliance.

You will manage the clinical staff at the site, assist in trial-related decisions, and participate in