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  3. Senior Clinical Research Associate (Bilingual) - Oncology - Canada (Remote)
WC

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

Worldwide Clinical Trials·Quebec

Full Time·Remote Ok·Remote friendly
·
5-10 yrs
·Posted 1 month ago
Practice for this role

About the role

Manage research activities at clinical sites, including site identification, start-up activities, and study maintenance. Conduct site initiation visits and ensure compliance with regulatory requirements and safety reporting.

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 university degree 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 [https://worldwide.wd1.myworkdayjobs.com/External]! For more information on Worldwide, visit www.Worldwide.com [http://www.Worldwide.com] or connect with us on LinkedIn [https://www.linkedin.com/company/worldwide-clinical-trials-inc-/].

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’re on a mission to hire the very best and 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.

Requirements

Requires a university or nursing degree and at least 5 years of experience as a CRA, specifically within Oncology. Must be fluent in both English and French and reside in Canada.

  • bachelor degree
  • Microsoft Office
  • Regulatory Compliance
  • Interpersonal Communication
  • Site Management
  • English Fluency
  • Clinical Research
  • Oncology
  • TMF Management
  • French Fluency
  • EDC Systems
  • CTMS
  • Study Initiation Visits

Posting details

Employment type
Full Time
Work arrangement
Remote Ok
Experience
5-10 yrs
Locations
Quebec; Ontario
Posted
Jul 8, 2026
Application
Employer website
WC

Hiring organization

Worldwide Clinical Trials

Worldwide Clinical Trials (Worldwide) is a global CRO serving development-driven biopharmaceutical companies, with more than 4,400 professionals operating across more than 70 countries. The company delivers therapeutically dedicated expertise in neuroscience, oncology, rare...

IndustryResearch Services
TypePrivately Held
Size1,001-5,000 employees
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Market context

Bilingual oncology CRA roles are selective

Senior Clinical Research Associate roles in oncology are typically in demand because sponsors need experienced monitors who can manage complex studies and site relationships. In Quebec, this role is especially competitive because employers often look for a university or nursing degree, deep oncology CRA experience, and strong English-French fluency, along with Canadian residency. Before applying, confirm your oncology monitoring history and bilingual qualifications align with the posting; this platform’s AI-summarized requirements and benefits help you review the original job description faster.

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