Parexel is a leading global clinical research organization that accelerates the development of life-saving treatments through innovative clinical trial solutions and regulatory expertise.
Raleigh, North Carolina
Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our 22,000+ global employees work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™ We continue to earn recognition industrywide, including the 2025 Scrip Award for “Best Contract Research Organization – Full-Service Provider,” 2024 Fierce Biotech CRO Award for "Innovative Approaches to Patient-Centric Research" and the 2024 and 2023 Society for Clinical Research Sites Eagle Award. Community Guidelines Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are: • Abusive, harassing or threatening to others. • Defamatory, offensive, obscene, vulgar or depicting violence. • Hateful targeting by race/ethnicity, age, color, creed, religion, gender, sexual preference or orientation, nationality or political beliefs. • Sexually explicit or pornographic. • Fraudulent, deceptive, libelous, misleading or unlawful. • Referencing criminal or illegal activity. • Spamming. We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.
Hybrid · Québec
The Clinical Trial Coordinator supports the Clinical Research Manager throughout the study life cycle, from start-up to closure. Responsibilities include managing essential documents, clinical supplies, regulatory submissions, and site budgets.
Remote · British Columbia, Canada
The Clinical Research Associate is responsible for managing site relationships, ensuring protocol compliance, and overseeing the quality and integrity of clinical trial data. They conduct various site visits, including qualification, initiation, monitoring, and termination, while protecting the rights and well-being of trial subjects.
Remote · Quebec, Quebec, Canada
The Clinical Research Associate is responsible for managing clinical site relationships, ensuring protocol compliance, and maintaining data integrity throughout the study lifecycle. They conduct various site visits, including qualification, initiation, monitoring, and termination, while protecting the rights and well-being of human subjects.
Remote · Ontario, Canada
Manage clinical trials or programs from initiation through closeout, overseeing vendors, sites, monitoring activities, study documentation, enrollment, and data-related processes. Ensure trials are conducted efficiently and in compliance with GCP, client procedures, FDA and ICH guidelines, while coordinating with cross-functional teams and stakeholders.
Hybrid · Québec
The Clinical Trial Coordinator supports the study lifecycle from start-up to closure, focusing on trial administration and document management. Key duties include managing site budgets, negotiating contracts, and coordinating regulatory submissions.