Clinical Research Associate - Vancouver, Canada - Translational Research in Oncology
Description
If you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you
Translational Research in Oncology (TRIO) is a global academic clinical research organization dedicated to advancing translational cancer research in the clinical trial setting.
TRIO is looking for a Clinical Research Associate
to join our Monitoring Resources team. Reporting to a CRA Line Manager
, this position will be home-based in Canada.
Responsibilities:
- Conducting site visits, including prestudy, 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 followup where applicable;
- Assisting with data validation and query resolution;
- Mentoring junior team members as required.
Qualifications:
- A minimum of 2 years of monitoring experience in oncology trials
- Experience monitoring phase 1 trials
- An advanced level of oncology knowledge
- Completion of a sciencerelated Bachelor's degree
- 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
What TRIO Can Offer You:
- Competitive salary
- 3 weeks of vacation plus paid Christmas Closure
- 2 weeks paid personal/sick time
- Health, Dental, Vision & Life Insurance premiums paid by TRIO
- Flexible working hours
- Monthly internet allowance
- Up to 5% RRSP Matching Program
Health & Safety:
Integrity - Teamwork - Passion
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