Medical Doctor at Harmony Clinical Research, Inc.

Harmony Clinical Research is actively seeking licensed physicians in Florida—across all medical specialties—who are passionate about entering the clinical research field as Principal Investigators (PIs). This role is ideal for MDs or DOs who are eager to diversify their practice, contribute to medical innovation, and help bring novel therapies to patients. As a PI, you will lead the clinical conduct of trials at our site(s), ensuring compliance, safety, and scientific integrity.

Success in this role looks like the timely and compliant execution of clinical trials, maintaining subject safety and data quality, while helping Harmony grow as a trusted research site for sponsors and CROs. The PI will work closely with our experienced operations team and have full support for training, trial startup, and patient recruitment.

• Oversee the clinical conduct of research studies in accordance with ICH-GCP, FDA regulations, IRB requirements, and protocol specifications
• Serve as the medical expert and primary clinical contact for all assigned clinical trials
• Ensure the safety and well-being of trial participants through appropriate medical oversight and decision-making
• Supervise the research team and delegate clinical tasks where appropriate
• Maintain accurate, timely, and complete source documentation and medical records
• Participate in sponsor and regulatory monitoring visits and audits
• Review and sign off on study documents including informed consent forms, adverse event reports, and case report forms
• Engage in protocol feasibility and site qualification visits as needed
• Collaborate with Harmony's leadership to improve trial conduct, recruitment strategies, and community outreach

• MD or DO with an active, unrestricted medical license in the state of Florida
• Board-certified or board-eligible in any specialty (Internal Medicine, Family Medicine, Pediatrics, Psychiatry, OB/GYN, Dermatology, etc. all welcome)
• Strong interest in clinical research and a commitment to participant safety and data quality
• Excellent verbal and written communication skills
• Ability to work collaboratively with cross-functional teams (coordinators, regulatory staff, sponsors, monitors)
• Prior research experience is preferred but not required—comprehensive training will be provided
• Must be able to commit time weekly to review subject progress and sign key study documents

As a Principal Investigator, you are the cornerstone of clinical trial execution at Harmony Clinical Research. You ensure that the science is sound, the subjects are safe, and the data is reliable. Your leadership helps position Harmony as a high-performing research site in our growing network, enabling us to attract exciting trials from top-tier sponsors and advance medical progress in our community.