Principal Investigator, Clinical Trials (PRN)
Company: BioTalent Agency
- Location: Miami, United States
- Seniority: Director
- Employment type: Contract
- Posted: Yesterday
- Offer language: English
Job description
🚀 Principal Investigator, Clinical Trials (PRN)
📍 Miami, FL | On-site
🗓 Part-Time | 20-30 Hours Per Week Guaranteed
🌱 Lead Innovative Clinical Research and Help Advance the Future of Medicine
🎓 Ideal opportunity for experienced Principal Investigators, Sub-Investigators, Physicians, and Clinical Research Leaders with hands-on clinical trial experience.
Are you passionate about clinical research, patient safety, and advancing innovative therapies? We're looking for a Principal Investigator, Clinical Trials (PRN) to provide medical oversight of clinical studies and ensure compliance with FDA regulations, GCP requirements, and study protocols while supporting a fast-paced Phase I clinical research environment.
🔬 What You'll Do
✔ Serve as the Principal Investigator overseeing clinical trial execution, patient safety, and protocol compliance
✔ Provide medical oversight for study participants and ensure appropriate assessment and management of adverse events
✔ Collaborate with research staff, sponsors, IRBs, and site leadership to ensure successful study execution
✔ Review study protocols, feasibility assessments, enrollment strategies, and recruitment plans
✔ Ensure compliance with FDA regulations, GCP guidelines, ICH requirements, and site SOPs
✔ Participate in investigator meetings, monitoring visits, audits, sponsor interactions, and regulatory inspections
✔ Support business development activities, protocol reviews, and sponsor relationship management
✔ Provide leadership, mentorship, and oversight to Sub-Investigators and clinical research staff
✅ What We're Looking For
🎓 M.D., D.O., or Ph.D. required
🧪 Previous clinical research experience required
🧪 Previous Principal Investigator or Sub-Investigator experience strongly preferred
🧪 Familiarity with clinical trial operations, protocol execution, and participant safety oversight
🧪 Strong understanding of FDA regulations, Good Clinical Practice (GCP), and ICH guidelines
🧪 Experience working within Phase I or other clinical research environments is highly desirable
🧪 Strong communication, presentation, negotiation, and stakeholder management skills
🧪 Ability to work effectively with sponsors, CROs, research staff, and regulatory agencies
🧪 Phase I clinical research environment
💰 Compensation
$140-$150 per hour
✅ PRN / Project-Based Opportunity
✅ 20-30 Hours Per Week Guaranteed
✅ 1-Year Engagement Contract
📍 Please Note
✅ On-site in Miami, FL
✅ Typically 2-3 days per week on-site
✅ Flexible schedule with hours open for discussion
✅ Phase I clinical research environment
✅ Opportunity to work with a dynamic and collaborative clinical research team
If this sounds like you, or someone in your network, I'd love to connect!
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