Clinical Research Associate – Canada

Resourcing Life Science; Canada; On-site; CAD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a dedicated Clinical Research Associate to monitor clinical studies in phases II-III. This role involves ensuring compliance with Good Clinical Practices and overseeing site initiation and close-out processes. The ideal candidate will have a Bachelor’s degree in life sciences and at least one year of monitoring experience within a CRO or pharmaceutical environment. Join a dynamic team that supports global pharmaceutical and biotech companies in their clinical development efforts, contributing to innovative healthcare solutions.

Qualifications

• Minimum 1 year monitoring experience as CRA within a CRO, Pharma, or Biotech.
• Experience in commercial studies and clinical studies phase II-III.

Responsibilities

• Monitoring clinical studies in phases II-III.
• Assuring adherence to Good Clinical Practices and compliance with study procedures.
• Supervising study conduct according to GCP requirements.

Skills

Monitoring clinical studies

Good Clinical Practices (GCP)

Site initiation

Site close out

Fluent English

Communication skills

Education

Bachelor degree in life-science

Job description

Company Description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA / Clinical Research Associate

Job Overview

• Monitoring clinical studies in phases II-III
• Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
• Identification, qualification and initiation of investigators and their sites.
• Supervising study conduct according to GCP requirements and all applicable laws.

Key Requirements

• Bachelor degree in life-science
• Min 1 year monitoring experience as CRA within a CRO, Pharma, Biotech in Germany
• Experience in commercial studies
• Experience with site initiation, site close out
• Experience in clinical studies phase II-III
• Fluent English
• Excellent communication skills
• A full clean drivers license
• FTE: 1.0

If you have difficulty in applying, have any questions or you cannot find what you are looking for please contact us on 0044 (0) 207 421 0000 or [e-mail]

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