Clinical Research Sub-Investigator / Site Director

ObjectiveHealth•Richmond, VA

23h•Onsite

About The Position

ObjectiveHealth 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. ObjectiveHealth is a clinical research company that uses proprietary technology to: Increase patient access to research trials within our communities, Provide physicians with enhanced care options for current patients, and Deliver superior clinical research enrollment metrics to Pharma sponsors All with the goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.

Requirements

Licensed Nurse Practitioner (NP) or Physician Assistant-Certified (PA-C) with an active license in the state of VA.
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.
This job requires legal authorization to work in the US. We are not currently accepting work visas.

Nice To Haves

Leadership experience in clinical or healthcare settings is preferred.

Responsibilities

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.