About Us
Avenue Research Group is a dedicated clinical research organization specializing in advancing dermatologic therapies through high-quality, patient-centered studies. Working alongside experienced investigators and healthcare professionals, the team conducts clinical trials across a wide range of skin conditions, helping to bring innovative treatments from development to real-world care. With a commitment to scientific integrity, operational excellence, and patient safety, Avenue Research Group plays a vital role in shaping the future of dermatology.
About You
You are a detail-oriented and organized clinical research professional with an interest in dermatology and clinical trials. You have experience supporting study operations, coordinating patient visits, maintaining regulatory documentation, and ensuring adherence to Good Clinical Practice and protocol requirements. You work well in a clinical setting, communicate effectively with patients and study teams, and take pride in delivering accurate, high-quality work. You are proactive, adaptable, and motivated to contribute to dermatologic research that improves patient care and advances innovative therapies.
Job Overview
We are seeking a dedicated Clinical Research Coordinator to join our team. This role is essential in managing and overseeing clinical trials, ensuring compliance with regulatory standards, and facilitating smooth study operations. The ideal candidate will possess strong organizational skills, medical knowledge, and experience in research settings. This position offers an opportunity to contribute to impactful medical research while working in a collaborative environment.
Duties
- Coordinate and manage clinical trial activities, including participant recruitment, scheduling, and follow-up
- Collect, record, and manage data accurately using established protocols and data management systems
- Perform phlebotomy procedures and assist with specimen collection
- Ensure adherence to study protocols, regulatory requirements, and ethical standards
- Maintain detailed documentation of study activities, adverse events, and protocol deviations
- Supervise research staff and volunteers to ensure quality and compliance in daily operations
- Communicate effectively with investigators, participants, sponsors and regulatory bodies
- Conduct analysis of collected data to support research objectives
- Provide training and supervision to junior staff or interns involved in the research projects
Requirements
- Recommended RN/BSc(Honours) or equivalent / proven experience in research coordination or related healthcare roles
- Strong knowledge of medical terminology and clinical trial processes regulations, ethics, and Good Clinical Practice (GCP)
- Experience with data collection, management, and analysis tools
- Certification or experience in phlebotomy is an asset
- Background in nursing or related medical fields is advantageous
- Excellent organizational and multitasking skills with attention to detail and accuracy
- Ability to work independently and collaboratively within a team environment
- Strong communication skills for effective interaction with participants and team members
- Experience with electronic data capture (EDC) systems
This position plays a vital role in advancing medical knowledge through rigorous research practices. Candidates should be committed to maintaining high standards of integrity, confidentiality, and professionalism throughout all aspects of their work.
This position plays a vital role in advancing medical knowledge through rigorous research practices. Candidates should be committed to maintaining high standards of integrity, confidentiality, and professionalism throughout all aspects of their work.
Benefits:
- In addition to base salary, there may be benefits available.
Pay: $49,920.00-$72,800.00 per year
Work Location: In person
