Clinical Research Associate

4 days ago

Québec, Canada Translational Research in Oncology Full time

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. Our passionate team is committed to providing cancer treatments of the future to the world of today.

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 Quebec.

**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.

**Qualifications**:

- A minimum of 2 years of monitoring experience in oncology trials
- Experience monitoring phase 1 trials
- An advanced level of oncology knowledge
- Fluent in French and English
- Completion of a science-related 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**

KxkvgQNsWs

  • Clinical Research Associate

    4 days ago

    Québec, Canada Institut de Cardiologie de Montréal Full time

    Clinical Research Associate (based in Montreal) **Clinical Research Associate (based in Montreal)** Position open to Canadian citizen esident or with Canadian work permit Montreal Health Innovations Coordinator Center Full Time The Montreal Health Innovations Coordinating Center (MHICC) is a full service contract research organization targeted on...

  • Clinical Advisor

    4 days ago

    Québec, Canada Clinical Research Dental Full time

    **Position Summary** This particular role is for an already established Territory in Greater Montreal. Fluent French and English is required. The **Clinical Advisor** (Dental) is accountable for developing sales and providing education within their assigned territory consistent with strategic and corporate goals and values. The role includes all facets of...

  • Clinical Trial Assistant

    15 hours ago

    Québec, Canada NeuroRx Research Full time

    **The role**:The Clinical Trial Assistant provides administrative support to all Project Managers in their daily duties, including liaising with clinical sites and MRI facilities. These duties include but are no limited to the following: - Submit requests for shipment of MRI supplies and trial-specific sFTP account creation - Issuing trial-specific...

  • Junior Clinical Research Coordinator

    2 weeks ago

    Québec, Canada Genge Partners, Inc Full time

    **Our Company** GENGE PARTNERS INC is an emerging clinical research unit specialized in late stage and real-world evidence trials. Equipped with 30+ years of experience, GENGE PARTNERS INC combines the expertise and quality assurance of a highly successful fully Health Canada accredited clinical research unit with the flexibility of a private organization...

  • Sr. Bilingual Clinical Research Associate

    5 days ago

    québec, Canada ICON Strategic Solutions Full time

    As a Sr. CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing:Ensuring regulatory, ICH-GCP and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific...

  • Sr. Bilingual Clinical Research Associate

    4 weeks ago

    Québec, QC, Canada ICON Strategic Solutions Full time

    As a Sr. CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Ensuring regulatory, ICH-GCP and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific...

  • Sr. Bilingual Clinical Research Associate

    4 weeks ago

    Québec, QC, Canada ICON Strategic Solutions Full time

    As a Sr. CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Ensuring regulatory, ICH-GCP and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific...

  • Sr. Bilingual Clinical Research Associate

    2 weeks ago

    Québec, QC, Canada ICON Strategic Solutions Full time

    As a Sr. CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Ensuring regulatory, ICH-GCP and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific...

  • Sr. Bilingual Clinical Research Associate

    2 weeks ago

    Québec, QC, Canada ICON Strategic Solutions Full time

    As a Sr. CRA you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Ensuring regulatory, ICH-GCP and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific...

  • Sr. Bilingual Clinical Research Associate

    5 days ago

    Québec City, Canada ICON Strategic Solutions Full time

    As a Sr. CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. What you will be doing: Ensuring regulatory, ICH-GCP and protocol compliance. Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific...