Evolution Research Group
Location
Little Rock, Arkansas
The Sub-Investigator provides clinical and medical oversight at the research site to ensure study protocols and regulatory standards are met. They are responsible for subject safety, data integrity, and collaborating with the Principal Investigator to manage clinical trial activities.
Candidates must be an APRN with an active medical license and possess a strong understanding of FDA regulations, GCP standards, and IRB requirements. Previous experience as a Sub-Investigator in industry-sponsored clinical trials is preferred.
Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.
Why join us? We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.
The Sub-Investigator serves as a secondary clinician responsible for clinical and medical oversight at the research site, acting on behalf of the Principal Investigator as needed. This role supports the execution of clinical trials in compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements while ensuring subject safety and data integrity.
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