A well-established clinical trial site based in Florida is seeking a Part-Time Principal Investigator (PI) to provide medical leadership and oversight of clinical trials. This position is ideal for a physician with prior research experience as a PI or Sub-Investigator, looking to contribute their expertise in a flexible, part-time capacity.
Key Responsibilities :
- Ensure the medical well-being and safety of study participants by supervising and conducting trials in accordance with FDA, ICH, NIH, GCP, HIPAA, study protocols, and site policies.
- Provide medical oversight for ongoing trials, including participant screening, eligibility assessment, and safety monitoring.
- Serve as the site's physician lead, maintaining compliance with all regulatory and ethical standards.
- Collaborate with study staff to support participant retention and successful study delivery.
- Maintain accurate documentation of study activities, adverse events, and protocol adherence.
- Foster strong relationships with sponsors, CROs, and internal teams.
- Represent the site at Investigator Meetings and support staff training on clinical trial protocols.
Requirements :
MD or DO degree with an active Florida medical license.Prior experience in clinical research (as a Principal Investigator or Sub-Investigator).Board certified in any medical specialty (internal medicine, family medicine, neurology, cardiology, nephrology, or other).Strong understanding of regulatory requirements and commitment to ethical research practices.Ability to balance clinical judgment with operational efficiency in a part-time roleThis is an excellent part-time opportunity for a physician to contribute to advancing clinical research while maintaining flexibility in their schedule. If you are committed to participant safety, scientific excellence, and collaborative teamwork, we encourage you to apply.
To apply, please send your updated resume to i.marland@x4lifesciences.com and let us know the best time to arrange a call.