Remote Oncology CRA — 1-Year Contract (Western Canada)

Translational Research in Oncology; Vancouver; Teletrabalho; CAD 110 000 - 138 000; Tempo integral

Resumo da oferta

Translational Research in Oncology (TRIO) is seeking a Clinical Research Associate (CRA) to join our Monitoring Resource team. This is a remote, full-time freelance opportunity on a 1-year contract, open to candidates based in Western Canada (British Columbia, Alberta, Saskatchewan, or Manitoba).

The CRA will perform data verification, conduct site visits, ensure compliance with FDA/ICH-GCP and local regulations, participate in budget negotiations, and mentor junior staff.

Qualificações

• 3+ years oncology CRA/CRC/Research Nurse experience.
• 1+ year monitoring in early-phase trials.
• Experience in solid tumor trials (breast, lung, gastric, ovarian, pancreatic) preferred.
• Fluent English; French desirable.
• Experience monitoring phase I trials valued.
• Willingness to travel up to 60%.

Responsabilidades

• Perform data verification of source documents.
• Conduct site visits (pre-study, initiation, monitoring, termination).
• Ensure adherence to FDA, ICH-GCP, and local regulations.
• Ensure implementation of FDA and ICH-GCP guidelines.
• Assist with budget negotiations and follow-up where applicable.
• Mentor junior team members and manage regulatory documents.

Conhecimentos

Oncology experience

Monitoring experience

Strong ICH-GCP knowledge

Clinical trial systems

Fluent English

French desirable

Willing to travel up to 60%

Bachelor’s degree in science

Formação académica

Science-related bachelor’s degree

Ferramentas

Clinical trial information systems

Descrição da oferta de emprego

Translational Research in Oncology (TRIO) is seeking a Clinical Research Associate (CRA) to join our Monitoring Resource team. This is a remote, full-time freelance opportunity on a 1-year contract, open to candidates based in Western Canada (British Columbia, Alberta, Saskatchewan, or Manitoba).

The CRA will perform data verification, conduct site visits, ensure compliance with FDA/ICH-GCP and local regulations, participate in budget negotiations, and mentor junior staff.