Sub l /Nurse Practitioner

About Company 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 including medical and dental coverage, a matching 401(k), and paid time off to recharge. Job Description 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. Key Responsibilities Conduct subject medical visits and oversee clinical aspects of active studies Support patient recruitment and enrollment efforts Ensure protocol adherence, informed consent compliance, and subject safety Evaluate and report adverse events per protocol and regulatory guidelines Collaborate with the Principal Investigator, study monitors, IRB, and site staff Participate in investigator meetings, monitoring visits, and audits Ensure accuracy, completeness, and timeliness of clinical trial data and documentation Oversee proper use and storage of investigational products Assist with study feasibility review and selectionCommunicate effectively with sponsors, research teams, and subjects Regulatory & Compliance Duties Maintain active medical licensure and current CV Sign required regulatory documents (FDA 1572, protocols, sponsor agreements) Ensure IRB approvals are obtained and maintained Uphold subject rights, welfare, and confidentiality Ensure compliance with GCP, ICH guidelines, and SOPs Qualifications APRN with active medical license required Experience as a Sub‑Investigator in industry‑sponsored clinical trials preferred Knowledge of FDA regulations, IRB requirements, and GCP standards Strong attention to detail and commitment to subject safety Ability to work collaboratively in a clinical research environment #J-18808-Ljbffr