Remote Clinical Research Associate (Oncology Trials)

Randstad Canada; Edmonton; Remote; CAD 100,000 - 123,000; Full time

Benefits offered by this job

Vacation 3 weeks

Personal time 10 days

Volunteer day

Health insurance

RRSP matching 5%

Flexible hours

Internet allowance

Home office allowance

Maternity top-up

Family assistance

Referral bonus

Job summary

Translational Research in Oncology (TRIO) invites applications for a Clinical Research Associate to support Monitoring Resources. The role is remote-based in Western Canada, with travel up to 60% and the opportunity to join a global org advancing translational cancer research.

We seek a candidate with a biology/health science background, 2+ years CRA experience, and solid knowledge of ICH-GCP, regulatory docs, and clinical trial systems. Fluency in English is required; French is a plus.

Qualifications

• Bachelor's Degree in allied health fields such as Medical, Nursing, Pharmacy, or Health Science – or its international equivalent.
• Minimum 2 years of previous CRA experience.
• Experience monitoring phase 1 trials.
• Excellent knowledge of medical terminology and clinical monitoring process.
• Strong ICH-GCPs knowledge.
• Experience with clinical trial information systems.
• Ability to travel up to 60% on average.
• Must work both independently and in a team environment.
• Read, write and speak fluent English required.
• Fluent in French is preferred, but not required.

Responsibilities

• Conducting 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

Skills

Clinical monitoring

ICH-GCP knowledge

Regulatory documentation

Team mentoring

Education

Bachelor's degree in allied health fields

Tools

Clinical trial information systems

Job description

Translational Research in Oncology (TRIO) invites applications for a Clinical Research Associate to support Monitoring Resources. The role is remote-based in Western Canada, with travel up to 60% and the opportunity to join a global org advancing translational cancer research.

We seek a candidate with a biology/health science background, 2+ years CRA experience, and solid knowledge of ICH-GCP, regulatory docs, and clinical trial systems. Fluency in English is required; French is a plus.