Principal Investigator (Clinical Research Physician)
Updated 10/14/25
$200,000
– $300,000
yearly
Shelby, Michigan, United States
Physician
Internal Medicine
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Job at a glance
Degree Required
MD/DO
Position Type
Full-Time
Work Environment
Clinic/Private Practice
Visa Sponsorship
No
Job description
Job description
We are looking for a physician with experience as a principal investigator to join a new clinical research site network conducting industry sponsored clinical trials in the areas of weight loss, diabetes, and other cardio metabolic diseases.
This is a full time, onsite, direct hire opportunity and a great chance to get in on the ground floor of a quickly growing organization
Job Responsibilities
We are seeking a dedicated and experienced Principal Investigator (PI) to lead clinical research trials in cardio-metabolic therapeutic areas. The PI will oversee and conduct Phase II–IV clinical studies, ensuring that all research activities adhere to regulatory guidelines, sponsor requirements, and the highest standards of patient safety and data integrity. This is a full-time, onsite, direct hire opportunity.
Key Responsibilities:
Serve as the medical lead and principal investigator for assigned clinical trials.
Provide medical oversight for study participants, including screening, enrollment, and ongoing clinical assessments.
Ensure compliance with study protocols, Good Clinical Practice (GCP), FDA regulations, and institutional policies.
Collaborate with clinical research staff to ensure accurate data collection, documentation, and reporting.
Review and sign off on case report forms, adverse event documentation, and other study-related data.
Communicate with sponsors, CROs, IRBs, and regulatory authorities as needed.
Provide medical expertise and guidance to study coordinators, sub-investigators, and site staff.
Contribute to the overall success and quality of the research program by maintaining high ethical and clinical standards.
Qualifications
MD or DO with an active, unrestricted medical license.
Minimum of 1 year of prior clinical research experience required.
Board certification in Internal Medicine, Cardiology, Endocrinology, or a related specialty preferred.
Strong knowledge of clinical trial processes, GCP, and regulatory requirements.
Excellent communication, leadership, and organizational skills.
Commitment to patient safety and scientific integrity.
Working Hours
Full time
By applying you agree to our Terms of Service