Oncology Clinical Research Associate - Remote Canada

Translational Research in Oncology; United States; À distance; USD 105 000 - 140 000; Plein temps

Avantages offerts par ce poste

Competitive salary

Vacation + Christmas closure

Personal/sick time off

Health Insurance

Flexible working hours

Internet allowance

RRSP matching

Résumé du poste

Translational Research in Oncology (TRIO) is seeking a Clinical Research Associate to join our Monitoring Resources team. The role is home-based in Canada and reports to a CRA Line Manager. You will conduct site visits, ensure regulatory compliance, and support data verification in oncology trials.

Requirements include at least 2 years monitoring in oncology, English and French fluency, experience with phase 1 trials, a science-related bachelor's degree, and ability to travel up to 60%.

Qualifications

• Minimum 2 years monitoring experience in oncology trials.
• Fluent in English and French.
• Experience monitoring phase 1 trials.
• Advanced oncology knowledge; science-related Bachelor's degree.
• Excellent knowledge of medical terminology and clinical monitoring process.
• Strong ICH-GCP knowledge.
• Willingness to travel up to 60%.

Responsabilités

• Conduct site visits, including pre-study, initiation, monitoring and termination.
• Confirming adherence to all FDA, ICH-GCP and local regulations.
• Ensuring the completion and collection of regulatory documents.
• Performing data verification of source documents.
• Ensuring implementation and compliance with FDA, ICH-GCP guidelines.
• Participating in budget negotiation and follow-up where applicable.
• Assisting with data validation and query resolution.
• Mentoring junior team members as required.

Connaissances

Monitoring experience

Oncology knowledge

Bilingual English/French

ICH-GCP knowledge

Travel up to 60%

Formation

Bachelor’s degree in science

Outils

Clinical trial information systems

Description du poste

Translational Research in Oncology (TRIO) is seeking a Clinical Research Associate to join our Monitoring Resources team. The role is home-based in Canada and reports to a CRA Line Manager. You will conduct site visits, ensure regulatory compliance, and support data verification in oncology trials.

Requirements include at least 2 years monitoring in oncology, English and French fluency, experience with phase 1 trials, a science-related bachelor's degree, and ability to travel up to 60%.