Clinical Research Coordinator

About Us

• Dermatology Research Institute specializes in clinical and epidemiological trials that focus on improving skin health. Founded by dermatologists, our team of accomplished physicians, trusted coordinators, and compassionate nurses are at the forefront of discovering new diagnostics and therapeutics. With a combined 11 years of experience, including over 100 unique studies for over 25 pharmaceutical companies, pediatric and adult patients can be certain they are receiving personalized solutions when it matters the most.
• Mission
• Statement: Dermatology Research Institutes takes great pride conducting industry-sponsored and investigator-initiated phase II, III, and IV studies for a broad spectrum of skin diseases and treatments in a fully equipped, state-of-the art facility with modern design, cutting-edge technology, efficient flow, and secure storage. We adhere to the most rigorous professional and ethical standards. Our highly-qualified staff pay meticulous attention to detail in terms of protocol compliance and data management, but also recognize the importance of creating a positive, safe, and comfortable environment for patients.

Vision

• Through consistency in meeting and/or exceeding enrolment targets as well as proficiency in presentation and publication of results, Dermatology Research Institute strives to become a respected leader for advancing medical knowledge. Contributing to scientific breakthroughs that will enhance the care of patients suffering from dermatologic conditions is what drives us.
• Core
• Values:
• Investigate
• Interpret
• Inform
• The
• Role
• Description: The Clinical Research Coordinator (CRC) serves as the lead coordinator on multiple concurrent clinical trials (up to 10 studies) and is responsible for the execution of study protocols and the delivery of high-quality clinical research data, while ensuring optimal patient care in accordance with Health Canada and ICH-GCP standards. This role is highly patient-facing and involves daily coordination of in-clinic patient visits, including screening, enrollment, and follow-up assessments. The CRC provides comprehensive oversight and coordination of clinical trials conducted at the
• Dermatology
• Research
• Institute, including: Acting as the primary point of responsibility for assigned studies, ensuring protocol adherence, regulatory compliance, and timely study execution Coordinating patient recruitment, screening, and enrollment, including conducting detailed eligibility assessments Leading daily patient visits, including study procedures, education, and ongoing participant support Obtaining and reviewing informed consent, ensuring patients receive and understand all study-related information Collecting, documenting, and managing clinical trial data with a high degree of accuracy and integrity Maintaining study documentation, source records, case report forms, and electronic databases Managing study timelines, resources, and competing priorities across multiple active trials Liaising with patients, investigators, nurses, administrative staff, and pharmaceutical sponsors to ensure seamless study conduct