Nurse Practitioner - Clinical Trial Sub-Investigator (PRN)

Evolution Research Group

Columbus (OH)

On-site

USD 138,000 - 179,000

Full time

14 days+
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Job summary

Evolution Research Group (ERG) is a neuroscience-focused clinical development company conducting Phase I–IV trials across the U.S. and beyond.

The Sub-Investigator serves as the secondary physician, supporting the Principal Investigator to ensure compliant, high-quality study execution at the site. Responsibilities include patient recruitment support, ensuring protocol and regulatory adherence, conducting visits, and coordinating with monitors while maintaining informed consent and data

Qualifications

  • NP licensed and in good standing with relevant board.
  • Experience as Sub-Investigator in industry-sponsored clinical trials preferred.
  • Strong knowledge of GCP, ICH guidelines, and regulatory requirements.
  • Knowledge of medical terminology and clinical research processes.

Responsibilities

  • Assist in recruitment of additional studies and input to protocols.
  • Ensure adherence to protocol and regulatory requirements.
  • Coordinate with monitors and investigators at the site.
  • Protect rights and welfare of subjects; manage informed consent processes.
  • Ensure data integrity and proper documentation across case report forms.

Skills

NP
Sub-Investigator experience
GCP/ICH knowledge
Medical terminology
Negotiation
Presentation
Communication
Travel ability

Education

NP credential
Industry-sponsored trial experience

Tools

Word
Excel
Study Manager

Job description

Evolution Research Group (ERG) is a neuroscience-focused clinical development company conducting Phase I–IV trials across the U.S. and beyond.

The Sub-Investigator serves as the secondary physician, supporting the Principal Investigator to ensure compliant, high-quality study execution at the site. Responsibilities include patient recruitment support, ensuring protocol and regulatory adherence, conducting visits, and coordinating with monitors while maintaining informed consent and data

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