CRA (Clinical Research Associate

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

Job summary

Groom & Associates is seeking a Clinical Research Associate (CRA) to support a global sponsor’s clinical trial. This remote role involves conducting site visits, ensuring compliance with regulations, and maintaining documentation. Ideal candidates have a Bachelor’s degree and at least 3 years of CRA experience, with strong communication skills and the ability to work independently.

Benefits

Flexible scheduling

Home-based work

Qualifications

• Minimum 3 years of CRA experience, preferably in multi-site or pharmaceutical-sponsored trials.
• Strong knowledge of ICH-GCP, Health Canada and FDA regulations.
• Comfortable working independently from a home office.

Responsibilities

• Conduct remote Site Initiation Visits (SIVs) and lead quarterly remote monitoring calls.
• Perform Close-Out Visits remotely and conduct on-site monitoring visits as needed.
• Ensure adherence to Good Clinical Practice (GCP) and maintain accurate monitoring documentation.

Skills

Communication

Time Management

Interpersonal Skills

Education

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

Job description

Job Title : Clinical Research Associate (CRA) – Ontario Region Location : Remote (Ontario-based) Type : Contract (until October 30, 2028) Start Date : As soon as possible Compensation : Commensurate with experience (hourly or fixed-price contract) About the Role Groom & Associates is seeking a detail-oriented and experienced Clinical Research Associate (CRA) to support a global sponsor’s ongoing clinical trial through remote and occasional on-site monitoring activities. The successful candidate will be home-based in Ontario and provide oversight for investigative sites in the region. Key Responsibilities Conduct remote Site Initiation Visits (SIVs) in accordance with study SOPs and regulatory requirements. Lead quarterly remote monitoring calls with each assigned site (approx. 3 contacts per year per site). Perform Close-Out Visits remotely as per study timelines. When required by the project team, conduct on-site monitoring visits (travel within Ontario). Ensure adherence to Good Clinical Practice (GCP) , study protocols, and sponsor expectations. Maintain complete, accurate, and timely monitoring documentation. Serve as a liaison between sponsor and site staff, facilitating communication and issue resolution. Qualifications Bachelor’s degree in life sciences, nursing, or a related field. Minimum 3 years of CRA experience , preferably in multi-site or pharmaceutical-sponsored trials. Strong knowledge of ICH-GCP , Health Canada and FDA regulations. Excellent communication, time management, and interpersonal skills. Comfortable working independently from a home office with occasional travel. Why Join Us? Join a high-impact study with a global sponsor. Work remotely with flexible scheduling and travel only when necessary.

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