Clinical Research Sub-Investigator / Site Director at ObjectiveHealth

Richmond, Virginia, United States -

Full Time

Start Date

Immediate

Expiry Date

12 Aug, 26

Salary

0.0

Posted On

14 May, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trial Coordination, Site Management, Patient Recruitment, Medical Assessment, GCP Compliance, ICH Guidelines, FDA Regulations, IRB Documentation, Performance Management, Staff Training, Adverse Event Reporting, Protocol Enforcement

Industry

Research Services

Description

Description 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. Who We Are 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. 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. Qualifications: 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. What We Offer Competitive compensation, 401(k) with Company match, a clear career pathway for advancement within the Company, Short- and Long-Term Disability, Health Savings and Flexible Spending Accounts, Health, Dental and Vision insurance Plans, Generous PTO, Adoption Assistance, Paid Holidays, and a wide selection of other voluntary benefits. Requirements This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant.

Responsibilities

Serve as a Sub-Investigator providing medical oversight and conducting physical examinations for clinical trials. Act as Site Director to manage day-to-day operations, staff performance, and site financial health.