Principal Investigator - Clinical Trials
Company: BioTalent Agency
- Location: Miami, United States
- Seniority: Senior
- Employment type: Part-time
- Posted: 2 days ago
- Offer language: English
Job description
📢 Principal Investigator (PRN) – Clinical Trials
📍 Location: Miami, FL
🕒 Schedule: Part-time | 20–30 hours per week | 2–3 days onsite
📋 Employment Type: W2 | PRN / Project-Based
📅 Engagement: Minimum 1 year - US Citizen - Greencard
We're partnering with a leading clinical research organization to find a Principal Investigator (PI) to support clinical trial operations at a Phase I research unit in Miami.
This is a great opportunity for a medical or research professional looking for a flexible, part-time engagement while contributing to meaningful clinical research.
The Principal Investigator will be responsible for overseeing clinical investigations, ensuring compliance with study protocols and regulatory requirements, protecting the rights and safety of research participants, and maintaining the integrity and quality of clinical trial data.
What we're looking for:
- MD, DO, or PhD - Florida Medical License
- 1 year of experience as a Principal Investigator (PI) or Sub-Investigator (Sub-I) preferred.
- Clinical research and clinical trial experience
- Knowledge of FDA regulations, GCP, and ICH guidelines
- Experience overseeing clinical trial protocols and ensuring patient safety and data integrity.
- Strong leadership and communication skills.
What makes this opportunity interesting?
- Part-time W2, PRN/project-based position.
- Minimum 1-year engagement.
- Guaranteed 20–30 hours per week.
- Flexible schedule, approximately 2–3 days per week.
- Competitive hourly compensation.
What You’ll Do
- Provide medical and scientific oversight of clinical trials, ensuring compliance with study protocols, FDA regulations, and Good Clinical Practice (GCP) guidelines.
- Oversee subject safety, informed consent, eligibility assessments, and medical decisions throughout clinical studies.
- Ensure the accuracy and integrity of clinical trial data and study documentation.
- Collaborate with Sub-Investigators, Site Directors, Study Coordinators, and research teams to ensure successful study execution.
- Support protocol feasibility assessments, recruitment strategies, and study enrollment goals.
- Maintain communication with sponsors, CROs, and Institutional Review Boards (IRBs).
- Maintaining PI credentials, licenses, CV and FDA Form 1572
If you're interested in exploring this opportunity or know someone who might be a great fit, I'd love to connect!
Work Authorization:
Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time
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