The base salary will be $63,730 - $90,820 per annum. Starting salary will be aligned with the successful candidate’s experience, skills, and demonstrated qualifications.

Please note, this is a wholly grant funded position.

About Western

Since 1878, Western University has been committed to serving our communities through the pursuit of academic excellence and by providing students, faculty, and community members with life-long opportunities for intellectual, social, and cultural growth. We seek excellent students, faculty, and staff to join us in what has become known as the "Western Experience" - an opportunity to contribute to a better world through the development of new knowledge, new abilities, new connections, and new ways to make a difference.

About Us

The Robarts Research Institute within the Schulich School of Medicine & Dentistry at Western University has made its mission to accelerate medical discovery. Through a powerful integration of basic and clinical research, we are driving major advances that impact on many of today's most devastating diseases.

The mission of the APILab is to transform outcomes in patients with asthma and COPD by accelerating patient-facing imaging physics discoveries, research and development and implementing/validating these findings in clinical and translational studies.

Responsibilities

The Regulatory and Clinical Research Coordinator will be responsible for supporting the operationalization of research studies under the direction of a Principal Investigator. The role will be responsible for the preparation, review, and management of submissions to local and national regulatory bodies for the purpose of research studies according to Good Clinical Practice (GCP)



and International Council for Harmonization of Technical Requirements of Pharmaceuticals for Human Uce (ICH) guidelines. The Coordinator will also lead the creation of responses required for the processing and approval of applications including Investigational Testing Authorizations, Clinical Trial Applications and local ethics submissions, including those required at hospital coordinating sites. The role will be a point of contact for internal and external inquiries related to the studies, coordinate and oversee the logistical and day-to-day activities, and will provide training for all staff members, collaborators and graduate students to plan, coordinate, and they will also execute all aspects of participant visits for research studies according to GCP guidelines. The Coordinator will be knowledgeable in all aspects of the studies and will design and conduct regular data and GCP audits to resolve any discrepancies within the data.

Qualifications

Education:

- Bachelor of Science (BSc) degree, Registered Respiratory Therapist (RRT), Registered (RN or BScN) or Practical Nurse (RPN) or equivalent education and experience

Experience:

- 2 years of experience supporting research studies in a research or clinical environment
- Previous clinical and clinical research experience




- 2 years regulatory experience including Health Canada and local ethics submissions preferred

Knowledge, Skills & Abilities:

- Familiarity with techniques for planning, managing and coordinating multiple projects, with competing priorities that involve a variety of stakeholders
- Knowledge of development and implementation of databases for research studies using REDCap
- Experience with electronic Common Technical Document (eCTD) format submissions, especially Class 2 medical device applications
- In depth knowledge of relational databases including database and form development, troubleshooting, and report design
- Understanding of research done in the field in order to make decisions for data management and database design
- Demonstrated ability to make decisions based on competing high priority tasks
- Ability to manage clinical data ensuring quality, accuracy, and consistency with clinical charts while maintaining confidentiality
- Ability to multi-task in a fast paced, clinical research environment
- Ability to write transparent, concise procedural and technical documentation for submission to regulatory bodies
- Ability to liaise between multiple departments in order to conduct daily research activities
- In depth knowledge of Good Clinical Practice and current ethical standards
- Ability to work in a collaborative research environment, and build and maintain lasting relationships with other departments, key partners, and external agencies
- Communication skills with the ability to converse with, write reports for, and deliver presentations to all levels of the organization
- Ability to write clear, concise and accurate procedural documentation
- Ability to ensure confidenti

📌 Regulatory and Clinical Research Coordinator (London)
🏢 Western University
📍 London