Join Bertucci Dermatology & MedSpa, led by Dr. Vince Bertucci, a global leader in cosmetic dermatology, and contribute to cutting-edge research that is shaping the future of skin health.
Role Overview:
The Clinical Research Intern will support the clinical research team in the coordination and execution of cosmetic dermatology clinical trials. Working under the direction of and reporting to Dr. Vince Bertucci and the lead Clinical Research Coordinator, the Clinical Research Intern will assist with study operations, participant coordination, and research documentation while learning about Good Clinical Practice (GCP), regulatory requirements, and clinical trial workflows. The studies include but are not limited to industry-sponsored clinical trials (Phase I-IV) with a variety of innovative drugs and/or devices.
This role offers valuable exposure to both clinical and administrative aspects of research, including participant interaction, data collection, and regulatory processes.
Key Responsibilities:
As a Clinical Research Intern, you will assist the research team in ensuring studies run smoothly, safely, and in compliance with regulatory standards. Responsibilities may include a combination of clinical support and administrative tasks.
Clinical Responsibilities:
- Assist with recruiting and screening potential study participants
- Support the research team during study visits and participant follow-ups
- Observe and assist with participant assessments and data collection
- Help document study procedures and participant information
- Assist with biospecimen collection preparation and processing
- Support study imaging requirements (e.g., capturing clinical photographs), as appropriate
- Assist with maintaining a clean and organized clinical environment
- Support clinic operations and patient flow during research visits
Administrative Responsibilities:
- Assist in maintaining study files, regulatory binders, and source documentation
- Support data entry into electronic data capture systems
- Assist with study scheduling and participant visit coordination
- Help prepare materials for research ethics board submissions
- Support communication with study participants and research team members
- Assist with organizing research documentation and tracking study timelines
- Assist with study start-up, monitoring, and close-out processes
Patient Experience:
- Assist in creating a welcoming and professional experience for study participants
- Support communication with patients in a respectful and professional manner
- Help ensure participants feel informed and supported throughout their study visits
- Maintain a polished and professional appearance reflecting the clinic’s standards
What We’re Looking For:
- Undergraduate degree in relevant field (e.g. Biology or Health Sciences)
- Currently enrolled and in good standing in a Clinical Research Diploma program
- Current and valid Division 5, GCP, and IATA certificates preferred
- Proficiency in electronic data capture systems and Microsoft Office
- Excellent organizational, communication, and interpersonal skills
- Ability to work independently and collaboratively in a fast-paced environment
- Meticulous attention to detail
- Excellent decision-making, analytical, and problem-solving skills
- Ability to understand, execute, and act on detailed instructions
Physical Requirements:
- Manual dexterity for handling medical instruments and devices
- Ability to stand for extended periods during clinical procedures or study visits
We offer:
- An engaging role in an exciting and growing industry working alongside a world-renowned dermatologist
- Mentorship from experienced clinical research professionals
- A culture based on values of integrity, passion, and excellence
- A positive, team-oriented, collaborative work environment
- Opportunities for professional development