Principal Investigator (MD/DO), Clinical Research

Principal Investigator, Clinical Research (MD/DO) $350,000-$400,000 Base Salary + Comprehensive Benefits Relocation Assistance Available Company Our client is one of the largest and most respected integrated clinical research site networks in the United States, conducting Phase I-IV clinical trials across CNS and psychiatry, neurology, dermatology, gastroenterology, pain, and other specialty indications. Position Summary This is a full-time physician position focused exclusively on clinical research. We are seeking a Principal Investigator with prior clinical research/trial experience who will provide medical oversight across a portfolio of Phase I-IV industry-sponsored clinical trials while working closely with an experienced team of clinical research coordinators, regulatory professionals, and site leadership. The incoming physician will step into active, well-supported research programs. This is not a ground-up build or a position where the physician is expected to create a research operation from scratch. You will inherit an established study pipeline, experienced research staff, and the support of a leading national site network. This is an opportunity for a physician to remain closely involved with patients and medical decision-making while building a long-term career at the forefront of clinical research. Responsibilities Serve as Principal Investigator for assigned industry-sponsored clinical trials Evaluate prospective study participants and determine eligibility Perform protocol-required medical assessments and oversee participant safety throughout each study Review adverse events, laboratory results, medical histories, concomitant medications, and other relevant clinical information Ensure trials are conducted in accordance with study protocols, ICH-GCP guidelines, FDA regulations, and applicable requirements Review and sign source documentation, study records, safety reports, and other required materials Provide medical guidance to clinical research coordinators and other members of the site team Collaborate with sponsors, CROs, medical monitors, and regulatory representatives Support patient enrollment, protocol compliance, data quality, and successful study execution Qualifications MD or DO degree Board-certified or Board Eligible US licensed Physician. Previous clinical research experience as a Principal Investigator, Sub-Investigator, research physician, or in a comparable capacity. Active Florida medical license or eligibility to obtain one DEA registration or ability to obtain one Working knowledge of ICH-GCP guidelines and clinical research regulations Strong clinical judgment and commitment to participant safety Previous experience serving as a Principal Investigator on industry-sponsored trials is preferred. Physicians with meaningful Sub-Investigator or clinical trial experience who are prepared to step into a full-time Principal Investigator position are also encouraged to apply. This full-time position offers a $350,000-$400,000 base salary , based on experience, along with a comprehensive benefits package that includes medical, dental, and vision insurance, a 401(k) retirement plan, paid time off, company holidays, and additional employer-sponsored benefits. Relocation assistance is available for qualified candidates . #J-18808-Ljbffr EPM Scientific