What are the responsibilities and job description for the Clinical Research Principal Investigator position at research institute group?
Job Title: Principal Investigator (PI) – Clinical Research
Location: Miami, Florida (on-site with potential for regional travel)
Employment Type: Contract or Part-Time/Full-Time (flexible based on study needs)
Overview
Our growing research clinic is seeking an experienced Principal Investigator to lead and oversee a variety of upcoming clinical research studies (Phase I–V) across multiple therapeutic areas. The PI will provide overall medical and scientific leadership, ensuring studies meet all ethical, regulatory, and protocol requirements.
Key Responsibilities
- Serve as the medical lead for all assigned studies, from start-up through close-out.
- Provide direct oversight of study participants’ safety, including eligibility assessments, adverse event evaluation, and medical management.
- Review and sign off on study protocols, informed consent forms, and other regulatory documents.
- Supervise and collaborate with sub-investigators, study coordinators, and other site staff to ensure compliance with GCP, FDA, and IRB requirements.
- Maintain accurate and timely documentation of all study activities and participant interactions.
- Participate in sponsor meetings, monitoring visits, and audits as required.
- Support business development by reviewing potential study feasibility and advising on new therapeutic areas.
Qualifications
- M.D. or D.O. with an active, unrestricted Florida medical license.
- At least 2–3 years of clinical research experience as a Principal or Sub-Investigator preferred; strong clinical background required.
- In-depth knowledge of Good Clinical Practice (GCP), FDA, and ICH guidelines.
- Excellent leadership, communication, and organizational skills.
- Ability to work with diverse patient populations and multiple therapeutic areas.
Preferred Skills
- Experience with early-phase (Phase I/II) trials.
- Familiarity with electronic data capture systems and clinical trial management software.
- Bilingual (English/Spanish) strongly preferred.
Compensation & Benefits
- Competitive compensation per study or salaried arrangement, commensurate with experience.
- Flexible schedule and opportunities to participate in a wide range of therapeutic research areas.
Job Types: Full-time, Part-time, Contract
Pay: $83,168.95 - $100,160.46 per year
Work Location: In person
Salary : $83,169 - $100,160