Clinical Research Associate (CRA)

Groom & Associés / Associates; Ontario; Remote; CAD 60,000 - 80,000; Full time

Job summary

Groom & Associates is seeking an experienced Clinical Research Associate (CRA) for a global clinical study in Ontario. This remote position involves monitoring sites, ensuring compliance with regulations, and requires a Bachelor's degree and significant CRA experience. Join a professional environment with competitive compensation and flexible working conditions.

Benefits

Flexible, remote-based model

Competitive compensation at $80 / hour

Limited travel required

Professional environment valuing expertise and independence

Qualifications

• Minimum 5–7 years of CRA experience with multi-site or late-phase studies.
• Deep knowledge of ICH-GCP, Health Canada, and FDA regulatory guidelines.
• Proven ability to work independently in a remote setting.

Responsibilities

• Conduct remote Site Initiation Visits (SIVs) and monitoring calls.
• Ensure adherence to Good Clinical Practice (GCP) and study protocols.
• Serve as the main liaison between the sponsor and clinical sites.

Skills

Communication

Time Management

Organizational Skills

Education

Bachelor’s degree in life sciences, nursing, or a related field

Job description

Job Title : Clinical Research Associate (CRA) – Ontario Region

Type : Contract (until end of 2028)

Start Date : As soon as possible

Compensation : $80 CAD / hour (incorporated consultant – invoicing model)

About the Role

Groom & Associates is seeking an experienced and proactive Clinical Research Associate (CRA) to support a global clinical study through a combination of remote and occasional on-site monitoring activities . This position is home-based in Ontario, with oversight responsibilities for investigative sites located in London, Ottawa, and Woodbridge . The workload will vary over time and is dependent on trial recruitment and progress .

Key Responsibilities

• Conduct remote Site Initiation Visits (SIVs) in compliance with study SOPs and regulatory requirements (1 per site)
• Lead quarterly remote monitoring calls (3 per year per site) to support data quality and protocol adherence
• Perform remote Close-Out Visits as defined by study timelines (1 per site)
• Conduct on-site monitoring visits on an as-needed basis, per project team requirements (travel within Ontario)
• Ensure strict adherence to Good Clinical Practice (GCP) , study protocols, and applicable Health Canada / FDA regulations
• Maintain timely, complete, and accurate monitoring documentation
• Serve as the main liaison between the sponsor and clinical sites, facilitating effective communication and issue resolution

Qualifications

• Bachelor’s degree in life sciences , nursing , or a related field
• Minimum 5–7 years of CRA experience , with a focus on multi-site or late-phase studies
• Experience with non-interventional or observational trials is considered an asset
• Deep knowledge of ICH-GCP , Health Canada, and FDA regulatory guidelines
• Strong communication, time management, and organizational skills
• Proven ability to work independently in a remote setting
• Must be incorporated and legally authorized to work in Canada as an independent contractor

Why Join Us?

• Be part of a high-impact global clinical study with a flexible, remote-based model
• Competitive compensation at $80 / hour , with a monthly invoicing structure
• Work from home with limited travel required only for site-specific needs
• Join a professional environment that values expertise, independence, and operational integrity