Global Clinix
Global Clinix is seeking a dedicated and experienced Principal Investigator (PI) with a background in Internal Medicine, Family Medicine, or any specialty to join our dynamic clinical research team.
This part-time role offers the opportunity to be at the forefront of clinical research while maintaining flexibility in your medical practice. The PI will play a pivotal role in ensuring protocol compliance, patient safety, and regulatory adherence while supporting the success and integrity of ongoing and future clinical trials.
Skills, Experience, Qualifications, If you have the right match for this opportunity, then make sure to apply today.
Key Responsibilities Ensure the safety and well-being of all study participants at the research site Review and evaluate participant medical histories for eligibility Conduct informed consent discussions and respond to participant questions thoroughly Perform physical examinations and medical evaluations as required Review laboratory and diagnostic data and provide clinical oversight Administer and/or oversee the administration of investigational products Remain knowledgeable on the investigational product via protocol, Investigator’s Brochure (IB), and sponsor documents Report serious adverse events (SAEs) and safety concerns in a timely and accurate manner to the sponsor and IRB Participate in all phases of site activity, including site qualification, initiation, monitoring, and close-out visits Ensure that subjects receive appropriate medical care and follow-up if the study is discontinued or terminated
Qualifications Valid M.D. or D.O. degree Active license to practice medicine in the state of Florida Preferred experience in clinical trials, either as a Principal Investigator or Sub-Investigator Strong understanding of Good Clinical Practice (GCP) and applicable FDA regulations Exceptional attention to detail and data accuracy Excellent communication and collaboration skills Bilingual (English/Spanish) preferred
Employment Details Part-time role: estimated 10–20 hours/week Flexible scheduling based on study needs and availability Compensation aligned with experience and market standards
Skills, Experience, Qualifications, If you have the right match for this opportunity, then make sure to apply today.
Key Responsibilities Ensure the safety and well-being of all study participants at the research site Review and evaluate participant medical histories for eligibility Conduct informed consent discussions and respond to participant questions thoroughly Perform physical examinations and medical evaluations as required Review laboratory and diagnostic data and provide clinical oversight Administer and/or oversee the administration of investigational products Remain knowledgeable on the investigational product via protocol, Investigator’s Brochure (IB), and sponsor documents Report serious adverse events (SAEs) and safety concerns in a timely and accurate manner to the sponsor and IRB Participate in all phases of site activity, including site qualification, initiation, monitoring, and close-out visits Ensure that subjects receive appropriate medical care and follow-up if the study is discontinued or terminated
Qualifications Valid M.D. or D.O. degree Active license to practice medicine in the state of Florida Preferred experience in clinical trials, either as a Principal Investigator or Sub-Investigator Strong understanding of Good Clinical Practice (GCP) and applicable FDA regulations Exceptional attention to detail and data accuracy Excellent communication and collaboration skills Bilingual (English/Spanish) preferred
Employment Details Part-time role: estimated 10–20 hours/week Flexible scheduling based on study needs and availability Compensation aligned with experience and market standards