Principal Investigator (MD/DO) Clinical Research -247365

Lead Principal Investigator (PI) – MD/DOLocation: Minneapolis, Minnesota 55403Employment Type: Direct Hire, W-2Schedule: Full-Time, Monday – Friday, 9:00 AM – 5:00 PMRelocation Assistance: Available for qualified candidatesAnnual Salary: $200,000 – $300,000Specialties Preferred: Neurology, Psychiatry, Family Medicine, Internal Medicine, Emergency MedicineAbout the OpportunityMedix is partnered with a multi-site clinical research organization supporting industry-sponsored pharmaceutical clinical trials. This Principal Investigator (MD/DO) opportunity is ideal for an experienced physician who is interested in partnering to launch and grow a new clinical research site , while leveraging the operational infrastructure, sponsor relationships, and support of an established research organization.This role offers a unique opportunity for a PI who enjoys hands-on clinical research , values high-quality patient care, and is motivated by the chance to help build a site from the ground up with long-term growth potential.OverviewThe Principal Investigator (MD/DO) serves as the medical and scientific lead for clinical trials conducted at the research site. The PI is responsible for ensuring subject safety, protocol compliance, data integrity, and regulatory adherence, while providing comprehensive medical oversight throughout the conduct of clinical studies.Key ResponsibilitiesServe as the Principal Investigator of record for assigned industry-sponsored clinical trialsProvide medical oversight and clinical decision-making for study participants, including management of comorbid conditionsEnsure trials are conducted in compliance with ICH-GCP, FDA regulations, IRB requirements, and sponsor protocolsPerform or supervise protocol-required clinical assessments and study proceduresReview and assess adverse events (AEs), serious adverse events (SAEs), and safety data, ensuring timely and accurate reportingLead and collaborate with sub-investigators, study coordinators, and site staffParticipate in site initiation visits, monitoring visits, audits, and inspectionsCommunicate effectively with sponsors, CROs, and regulatory authoritiesMaintain accurate and complete source documentation and regulatory filesContribute to the development, growth, and long-term success of a newly launched research siteRequired QualificationsMD or DO with board certification (or eligibility) in Neurology, Psychiatry, Family Medicine, Internal Medicine, or Emergency MedicineActive, unrestricted Minnesota medical license, or eligibility to obtainDemonstrated experience serving as a Principal Investigator on industry-sponsored pharmaceutical clinical trials (required)Strong understanding of clinical research regulations, GCP, and FDA requirementsInterest in partnering with an established clinical research organization to launch and build a new site from the ground upExcellent communication, leadership, and collaborative skillsWhy This Role Is UniqueOpportunity to help launch and shape a new clinical research siteBacked by the infrastructure, operational support, and sponsor relationships of an established multi-site organizationAbility to expand long-term involvement in clinical research and site leadershipMeaningful impact on patient access to innovative therapiesInterested in learning more about this opportunity or exploring other Principal Investigator opportunities with Medix nationwide? Apply today to start the conversation.