What are the responsibilities and job description for the Principal Investigator (MD/DO) - Part-Time position at ObjectiveHealth?
Description
Principal Investigator - Part-Time
ObjectiveHealth is seeking a board-certified MD or DO to serve as a Part-Time Principal Investigator at our Dayton, OH research site. This is a unique opportunity for a physician in Internal Medicine or Family Medicine 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
Key Responsibilities
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
Principal Investigator - Part-Time
ObjectiveHealth is seeking a board-certified MD or DO to serve as a Part-Time Principal Investigator at our Dayton, OH research site. This is a unique opportunity for a physician in Internal Medicine or Family Medicine 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
Key Responsibilities
- Serve as the Principal 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.
- MD or DO with a valid and active medical license in the state of Ohio with no history of license suspension or disbarment.
- Board certification in Internal Medicine or Family Medicine (additional specialty certifications are welcome).
- Prior clinical research experience is preferred but not required.
- Strong attention to detail and a demonstrated commitment to high ethical standards.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively in a team-based environment.
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