Phase II-III Monitoring CRA — Global CRO

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

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.