Details:
- Compensation: $250 - $350k
- Benefits: Medical, Dental, Vision
- Employment Classification: Direct Hire
- Status: On-Site
- Job ID: 21398
Job Title: Principal Investigator- Internal Medicine
Work Location: Hillsborough County, Florida
Summary:
This full-time position offers a competitive salary range and relocation assistance. The Principal Investigator will oversee and conduct clinical trials, ensuring compliance with protocols, regulatory standards, and participant safety. The role involves collaboration with research teams and regulatory personnel, management of research integrity, and oversight of compliance, financial, and personnel aspects of clinical projects.
Responsibilities:
- Lead clinical trials as Principal Investigator, ensuring adherence to research protocols and regulatory standards.
- Maintain active medical licensure and board certification, and complete all required training and certifications for clinical research protocols.
- Evaluate and enroll participants based on protocol-specific criteria, ensuring informed consent and participant safety throughout the study.
- Oversee and delegate responsibilities to clinical research staff, providing education on study protocols and investigational products.
- Monitor participant responses, assess adverse events, and ensure accurate documentation and reporting as required by protocols.
- Collaborate with study teams and leadership to meet recruitment goals, project budgets, and overall research objectives.
- Attend investigator meetings, educational seminars, and maintain up-to-date knowledge of clinical research best practices.
- Perform additional duties as assigned, ensuring the integrity and compliance of all aspects of the research project.
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 relevant role.
- Strong knowledge of Good Clinical Practice (GCP), ICH guidelines, and clinical research protocols.
- Experience with drug delivery systems and ability to prepare injections, infusions, etc.
- Excellent organizational, communication, and record-keeping skills.
- Ability to work independently and as part of a team, with strong attention to detail and the ability to respond effectively in emergency situations.
Published Category: Clinical Research