Job Title: Principal Investigator- Internal Medicine

Work Location: Broward County, Florida

Summary:

This full-time position offers a competitive salary range and relocation assistance. The Principal Investigator is responsible for overseeing clinical trials, ensuring compliance with protocols, regulatory standards, and participant safety. The role involves collaboration with research teams and regulatory personnel, management of research projects, and maintaining the integrity of all trial-related activities.

Responsibilities:

• Lead and oversee clinical trials, ensuring adherence to research protocols, Good Clinical Practices (GCP), and regulatory requirements.
• Maintain active medical licensure and board certification, and serve as Principal Investigator throughout the duration of assigned studies.
• Collaborate with study teams and regulatory personnel to ensure participant safety and data integrity.
• Evaluate and recruit participants based on protocol-specific criteria, and conduct necessary clinical assessments and documentation.
• Train and supervise research staff, ensuring proper delegation and understanding of study protocols and investigational products.
• Monitor participant safety, assess responses to investigational therapies, and report adverse events and protocol deviations as required.
• Manage project budgets, attend investigator meetings, and contribute to the achievement of organizational research goals.
• Ensure informed consent is obtained and maintained, and fulfill all documentation and reporting obligations throughout the trial.

Qualifications:

• Valid M.D. or D.O. degree; Board Certified or Board Eligible.
• Active DEA license or ability to obtain one.
• Active license to practice medicine in Florida, or ability to obtain one.
• 1-3 years of experience conducting clinical research trials as a Principal Investigator, Sub-Investigator, or in a related capacity.
• Strong knowledge of clinical research protocols, GCP/ICH guidelines, medications, and general medical conditions.
• Experience with drug delivery systems and clinical trial procedures.
• Excellent organizational, communication, and documentation skills.
• Ability to work independently and collaboratively, maintain effective relationships, and respond effectively in emergency situations.

Published Category: Clinical Research