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Clinical Trials Jobs in Quebec (NOW HIRING)

These clinical trials will cover the full range of neurologic disorders. Essential Functions The role includes predominantly Medical Monitoring responsibilities with Medical Strategic input ...

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. * Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.

Monitor financial activity for clinical trials and ensure payments are received by the sponsor and invoices are paid to suppliers, in a timely manner. * Follow up with sponsors on arrears and report ...

New

Monitor financial activity for clinical trials and ensure payments are received by the sponsor and invoices are paid to suppliers, in a timely manner. * Follow up with sponsors on arrears and report ...

New

The Clinical Research Unit (CRU) of the Montreal Neurological Institute-Hospital (the Neuro) conducts over 120 clinical trials and clinical research projects in adult neuroscience. Project Leads ...

The Clinical Research Unit (CRU) of the Montreal Neurological Institute-Hospital (the Neuro) conducts over 120 clinical trials and clinical research projects in adult neuroscience. Project Leads ...

Contribute to improving screening and tracking workflows, including identifying candidates for imaging studies and relevant clinical trials. (iv) Contact participants outside of clinic, including ...

Research Assistant 1

Montreal, QC · On-site

CA$30.54/hr

Contribute to improving screening and tracking workflows, including identifying candidates for imaging studies and relevant clinical trials. (iv) Contact participants outside of clinic, including ...

Research Technician

Montreal, QC · On-site

CA$33.05 - CA$40.97/hr

The Clinical Research Unit (CRU) of the Montreal Neurological Institute-Hospital ( The Neuro ) conducts over 100 clinical trials for patients with neurological disorders. The CRU is looking to hire a ...

Research Technician

Montreal, QC · On-site

CA$33.05 - CA$40.97/hr

The Clinical Research Unit (CRU) of the Montreal Neurological Institute-Hospital ( The Neuro ) conducts over 100 clinical trials for patients with neurological disorders. The CRU is looking to hire a ...

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Clinical Trials information

What are the key skills and qualifications needed to thrive in a clinical trials position, and why are they important?

To thrive in Clinical Trials roles, you need a strong understanding of clinical research principles, Good Clinical Practice (GCP) guidelines, and a background in life sciences or healthcare. Familiarity with electronic data capture (EDC) systems, regulatory compliance software, and relevant certifications such as GCP or CCRA is highly valuable. Attention to detail, organizational skills, and effective communication enable collaboration across multidisciplinary teams. These competencies are crucial for ensuring protocol adherence, data integrity, and the successful execution of trial activities.

What are some common career paths or advancement opportunities for professionals working in clinical trials?

Many professionals in Clinical Trials start their careers as Clinical Research Coordinators, Clinical Research Associates, or Data Managers. With experience, you can advance to roles such as Senior Clinical Research Associate, Clinical Trial Manager, or Project Manager, and potentially move into areas like regulatory affairs, medical writing, or quality assurance. The role offers continuous learning opportunities, exposure to innovative therapies, and often provides the chance to lead larger, more complex studies as you progress. Advancement is typically supported by additional certifications, strong performance, and a proactive approach to professional development. Teamwork and networking within the industry can also open new doors for growth.

What is a clinical trial?

A Clinical Trials job involves managing, coordinating, or supporting research studies that evaluate the safety and effectiveness of medical treatments, drugs, or devices. Professionals in this field work on trial design, patient recruitment, data collection, regulatory compliance, and reporting results. Roles can range from clinical research coordinators to trial managers and regulatory specialists. The goal is to ensure that studies follow ethical guidelines and produce reliable data for medical advancements.

What are the most commonly searched types of Clinical Trials jobs in Quebec? The most popular types of Clinical Trials jobs in Quebec are:
What are popular job titles related to Clinical Trials jobs in Quebec? For Clinical Trials jobs in Quebec, the most frequently searched job titles are:
What job categories do people searching Clinical Trials jobs in Quebec look for? The top searched job categories for Clinical Trials jobs in Quebec are:
Infographic showing various Clinical Trials job openings in Quebec as of August 2026, with employment types broken down into 14% As Needed, and 86% Full Time. Highlights an 65% In-person, and 35% Remote job distribution.

Senior Clinical Research Associate (Bilingual) - Oncology - Canada (Remote)

Worldwide Clinical Trials

Quebec, QC

Full-time

Re-posted 4 days ago


Job description

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What Clinical Operations does at Worldwide

At Worldwide Clinical Trials, we invite you to embark on a rewarding journey within Clinical Operations, where your contributions will leave a profound impact on the lives of patients.

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture. Our commitment to advancing clinical research is nurtured within a supportive and team-oriented environment. In a CRA role, you'll receive extensive support through regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs.

Through regular touchpoints and coaching conversations with your Line Manager, we ensure that your professional development remains a top priority. We offer a clear career path and development that can lead to Clinical Trial Manager roles. We take pride in our accessible Executive Leadership team, who are equally committed to advancing science and surmounting obstacles to make a difference in the lives of patients around the world.

We offer an unparalleled experience, where you can drive remarkable scientific breakthroughs and be at the very core of every successful clinical trial. Experience a world of difference with us at Worldwide!

What you will do

  • Responsible for managing the research activities at sites participating in Worldwide's clinical research projects

  • Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded

  • Conduct study initiation visits (SIVs)

  • While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements

What you will bring to the role

  • Excellent interpersonal, oral, and written communication skills in English

  • Superior organizational skills with attention to detail

  • Ability to work with little or no supervision

  • Proficiency in Microsoft Office, CTMS, and EDC Systems

Your experience

  • 5+ years of experience as a Clinical Research Associate

  • 4-year universitydegree OR Nursing Degree

  • Experience in Oncology is required

  • Fluent in written and verbal English and French is required

  • Candidates must reside in Canada

  • Willingness to travel regionally required

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We'reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.