Sub Investigator (NP/PA-C) - Part-Time

ObjectiveHealth•Dayton, OH

30d•Onsite

About The Position

ObjectiveHealth is seeking a licensed Nurse Practitioner (NP) or Physician Assistant-Certified (PA-C) to serve as a Part-Time Sub-Investigator at our Dayton, OH research site. This is a unique opportunity for an advanced practice provider in Internal Medicine, Family Medicine, or a related field to contribute to innovative clinical research while maintaining a flexible schedule. ObjectiveHealth is a clinical research company transforming how research is conducted at the point of care. Using our proprietary technology, we aim to: Increase patient access to research trials within our communities Provide physicians with enhanced care options for current patients Deliver superior clinical research enrollment metrics to Pharma sponsors All with the ultimate 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 Ohio.
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.
ObjectiveHealth is an EEO Employer and an E-Verify participant

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.