What are the responsibilities and job description for the Physician/Principal Investigator (Clinical Research) position at Avanti Clinical Research Corp.?
Job Title: Principal Investigator (Medical Research)
Location: Hialeah, FL
Department: Clinical Research / R&D
Reports To: Director of Research / Chief Scientific Officer
Employment Type: Full-Time/Part Time
About the Company:
Avanti Clinical Research Corp. is a leading medical research organization committed to advancing healthcare through innovative research, clinical trials, and translational science. Our mission is to bring life-changing therapies and diagnostics from bench to bedside, improving outcomes for patients worldwide.
Position Overview:
We are seeking an experienced and motivated Principal Investigator (PI) to lead and oversee clinical and/or translational research studies. The PI will be responsible for the scientific and ethical integrity of research protocols, ensuring regulatory compliance, and managing multidisciplinary project teams. This role plays a critical part in designing studies, securing funding, publishing results, and translating scientific discoveries into clinical applications.
Key Responsibilities:
- Design, develop, and execute research protocols in alignment with company goals and regulatory standards.
- Lead and manage clinical trials, observational studies, or laboratory-based research projects.
- Serve as the primary point of contact for regulatory bodies (e.g., IRB, FDA), sponsors, and collaborators.
- Oversee data collection, analysis, and interpretation; ensure accuracy and scientific rigor.
- Prepare and submit grant applications, study reports, manuscripts, and regulatory documents.
- Mentor and supervise research staff, including scientists, coordinators, and students.
- Collaborate with cross-functional teams including clinical operations, biostatistics, regulatory affairs, and medical writing.
- Ensure all research activities are conducted in compliance with Good Clinical Practice (GCP), institutional policies, and applicable regulations.
- Present findings at scientific conferences and contribute to publications in peer-reviewed journals.
Qualifications:
Required:
- MD or PhD in a relevant biomedical or clinical science field.
- Minimum of 1-3 years of experience leading clinical or biomedical research projects.
- In-depth understanding of clinical trial design, GCP, and regulatory requirements.
- Excellent leadership, organizational, and communication skills.
Preferred:
- Board certification (if applicable) and clinical experience in a relevant therapeutic area.
- Particularly interested in candidates with expertise in Internal Medicine, Psychiatry, Neurology, Pulmonology, Immunology, Nephrology, Dermatology, and Oncology.
What we Offer:
- Competitive compensation per study and performance-based bonuses
- Opportunities for career advancement and continued education
- Collaborative, mission-driven work environment
- Flexible work options
Job Types: Full-time, Part-time
Benefits:
- Flexible schedule
Work Location: In person