Clinical Research Associate (CRA)

Groom & Associés / Associates; Ontario; Remote; CAD 70,000 - 90,000; Full time

Job summary

A leading company is seeking a detail-oriented Clinical Research Associate (CRA) to support a global sponsor’s clinical trial in Ontario. The successful candidate will conduct remote monitoring and occasional on-site visits, ensuring compliance with regulatory standards. This role offers flexibility with home-based work and a chance to contribute to impactful studies.

Benefits

Flexible scheduling

Work remotely

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.

Responsibilities

• Conduct remote Site Initiation Visits (SIVs) in accordance with study SOPs.
• Lead quarterly remote monitoring calls with each assigned site.
• Ensure adherence to Good Clinical Practice (GCP) and study protocols.

Skills

Communication

Time Management

Interpersonal Skills

Education

Bachelor’s degree in life sciences

Bachelor’s degree in nursing

Job description

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

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.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Research and Project Management

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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