Clinical Research Associate

Groom & Associés / Associates; Electoral Area A; Remote; CAD 60,000 - 80,000; Full time

Job summary

A leading company in clinical research is seeking a Clinical Research Associate (CRA) to support a global clinical study. This remote position requires strong organizational skills and a solid understanding of regulatory frameworks, with responsibilities including remote monitoring and site visits across British Columbia.

Benefits

Flexible remote work

Competitive compensation

Professional network support

Qualifications

• Minimum 5–7 years of CRA experience, preferably in multi-site or late-phase studies.
• Solid understanding of ICH-GCP, Health Canada, and FDA regulatory frameworks.
• Must be incorporated and authorized to work in Canada as an independent contractor.

Responsibilities

• Conduct remote Site Initiation Visits (SIVs) and lead quarterly remote monitoring calls.
• Ensure compliance with Good Clinical Practice (GCP) and regulatory requirements.
• Act as a primary liaison between the sponsor and site staff.

Skills

Communication

Organizational Skills

Independence

Education

Bachelor's degree in life sciences, nursing, or related field

Job description

Job Title : Clinical Research Associate (CRA) – British Columbia Region

Location : Remote (British Columbia-based)

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 an ongoing global clinical study through a combination of remote and occasional on-site monitoring activities . This position is home-based in British Columbia, with oversight responsibilities for investigative sites located in Vancouver, Kelowna, and New Westminster . The workload will vary over the course of the project and is closely tied to trial progress and patient recruitment .

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 ensure ongoing compliance and data integrity
• Perform remote Close-Out Visits according to study timelines (1 per site)
• Conduct on-site monitoring visits on an ad hoc basis , if required by the project team (travel within British Columbia)
• Ensure strict adherence to Good Clinical Practice (GCP) , study protocols, and applicable Health Canada / FDA regulations
• Accurately maintain and submit all monitoring documentation in a timely manner
• Act as a primary liaison between the sponsor and site staff to facilitate effective communication and resolution of issues

Qualifications

• Bachelor's degree in life sciences , nursing , or a related field
• Minimum 5–7 years of CRA experience , preferably in multi-site or late-phase studies
• Prior experience with non-interventional or observational studies is considered a strong asset
• Solid understanding of ICH-GCP , Health Canada, and FDA regulatory frameworks
• Excellent written and verbal communication skills
• Strong organizational skills with the ability to work independently from a remote setting
• Must be incorporated and authorized to work in Canada as an independent contractor

Why Join Us?

• Support a high-impact global study in a dynamic and collaborative setting
• Enjoy the flexibility of remote work , with travel limited to essential on-site visits
• Competitive compensation at $80 / hour , with monthly invoicing structure
• Be part of a professional network that values quality, autonomy, and operational excellence

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