Details:
- Compensation: $80 - $110k
- Benefits: Medical, Dental, Vision
- Employment Classification: Direct Hire
- Status: On-Site
- Job ID: 21440
Sub-Investigator / Site Director
Richmond, VA
Our Client is seeking a highly skilled Sub-Investigator / Site Director to join our dynamic clinical research team in Richmond, VA. This role serves as both a clinical and operational leader within the site. Under the supervision of the Principal Investigator, the Sub-Investigator will contribute to the coordination of clinical trials while also acting as Site Director, overseeing day-to-day site operations and research staff.
Essential Functions
Richmond, VA
Our Client is seeking a highly skilled Sub-Investigator / Site Director to join our dynamic clinical research team in Richmond, VA. This role serves as both a clinical and operational leader within the site. Under the supervision of the Principal Investigator, the Sub-Investigator will contribute to the coordination of clinical trials while also acting as Site Director, overseeing day-to-day site operations and research staff.
Essential Functions
- Serve as the Sub Investigator for assigned clinical trials, ensuring overall study oversight.
- Oversee and enforce compliance with study protocols while prioritizing subject safety at all times.
- Conduct and document physical examinations and medical assessments in accordance with research protocol requirements.
- Provide continuous medical oversight throughout all phases of the clinical trial lifecycle.
- Collaborate effectively with study coordinators, site staff, and other research team members to ensure smooth study execution.
- Participate in sponsor meetings, site initiation visits, monitoring visits, and audits as needed.
- Maintain strict compliance with GCP, ICH guidelines, FDA regulations, and internal SOPs.
- Lead and develop site staff through ongoing training, performance management, and regular 1:1s while maintaining strong communication with investigators, sponsors, and internal teams.
- Manage day-to-day study execution including patient recruitment, scheduling, visits, and coordination of clinical and administrative workflows.
- Support direct patient care procedures, oversee adverse event reporting and protocol deviations, and ensure proper IRB and study documentation compliance.
- Own site performance including enrollment, visit targets, and overall financial health.
- Ensure all clinical trial activities follow protocols, GCP, IRB, and regulatory requirements, including audit readiness, accurate documentation, and timely data entry.
- Licensed Nurse Practitioner (NP) or Physician Assistant-Certified (PA-C) with an active license in the state of VA.
- Leadership experience in clinical or healthcare settings is preferred.
- Ability to perform study-related clinical assessments and procedures under the guidance of the Principal Investigator.
- Strong attention to detail and commitment to maintaining high ethical, clinical, and regulatory standards.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively in a multidisciplinary research environment.