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Principal Investigator; Psychiatry

Job in Northern, Floyd County, Kentucky, USA
Listing for: Emvenio Research, Inc
Full Time position
Listed on 2026-10-07
Job specializations:
  • Science
    Clinical Research
Salary/Wage Range or Industry Benchmark: 156600 - 266700 USD Yearly USD 156600.00 266700.00 YEAR
Job Description & How to Apply Below
Position: Principal Investigator (Psychiatry)
Location: Northern

** Put your talents to work at PCM!
** Whether you work in our Home Care, Clinical Research, Impairments, or Catastrophic Care division, you will support our mission to deliver care and other services that enhance the quality of life of our clients. Be a part of our dynamic client-focused team and make a difference in your career!
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** This is a 1099 Independent Contractor position.
** The typical base pay range for this role is USD $156,600 - $266,700 per year.

Individual base pay depends on various factors, in addition to primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience, skills and other market-based factors.
** Available Benefits Include
*** Medical* Dental
* Vision* 401(k)
* Company Paid Short Term Disability
* Flexible Spending Account (FSA)
* Health Savings Account (HSA)
* Paid Time Off
* Voluntary Benefits   Please contact Carson Moreira-Rego at  x387 or ei today to learn more about our opportunities where you can make a difference in your own career!

Professional Case Management is an Equal Opportunity Employer.

The Principal Investigator (PI) is responsible for conducting objective clinical research that generates independent, high quality and reproducible results.  The PI is charged with the management and integrity of the design, conduct and reporting of the research project and for managing, monitoring and ensuring the integrity of any collaborative or delegated relationships.  Additionally, the PI is responsible for the direction and oversight of compliance, financial, personnel and other related aspects of the research project and for coordination with necessary departments to assure the research is conducted in accordance with federal regulations and sponsoring agency policy and procedures.
*
* QUALIFICATIONS:

*** A valid medical degree (MD or DO).
* 5+ years of clinical research experience as a PI or Sub-Investigator
* Proficient with Microsoft Office Suite
* An active medical license in good standing, with unrestricted ability to practice in place of work, where applicable.
* Demonstrated leadership skills, including strong communication, presentation, written and interpersonal skills.
* Proven ability to be highly collaborative and quickly establish credibility and gain participation across a variety of stakeholders, both internal and external.
* Results-driven, with a track record of building, managing and motivating teams to meet or exceed clinical goals and objectives.
* Strong analytical and decision-making capabilities that support clinical continuous improvement initiatives.
* Advanced organizational and project management abilities, including the ability to work within tight deadlines on a range of projects.
* Must be a self-starter and highly motivated individual who can identify needs and proactively work to solve problems and gaps.
** ESSENTIAL FUNCTIONS/AREAS OF ACCOUNTABILITY:
*** Risks to research subjects are minimized by using procedures which are consistent with sound research design and which do not unnecessarily expose the subjects to risk; and, whenever appropriate, by using procedures already being performed on the subjects for diagnostic or treatment purposes;
* Risks to human research subjects are reasonable in relation to the anticipated benefits (if any) to the individual, and the importance of the knowledge that may be expected to result;
* Selection of human subjects and patients for research participation is equitable;
* Individuals are adequately informed of the risks and benefits of research participation and the procedures that will be involved in the research, and that informed consent will be obtained from each prospective human research subject, or his/her legally authorized representative, in…
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