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.
Remote · Quebec, Quebec, Canada
The Clinical Research Associate is responsible for managing clinical site relationships, ensuring protocol compliance, and maintaining data integrity throughout the clinical trial process. They conduct site visits, oversee patient safety, and develop recruitment strategies to meet project timelines.
Remote · British Columbia, Canada
The Senior Clinical Research Associate is responsible for the site management, monitoring, and close-out of clinical trial sites to ensure patient safety and protocol compliance. They act as the primary point of contact for investigator sites, facilitating communication and resolving operational issues throughout the study lifecycle.
Remote · Ontario, Canada
The Study Operations Manager oversees clinical trial activities from startup through conduct and closeout, ensuring operational delivery and adherence to project plans. They lead local study teams, manage vendor relationships, and coordinate with regulatory bodies to ensure compliance and timely milestone achievement.
Remote · Quebec, Quebec, Canada
The Clinical Research Manager is accountable for end-to-end project management and performance of assigned protocols in compliance with ICH/GCP and country regulations. This includes acting as the main point of contact between country operations and clinical trial teams while managing site selection, recruitment, and closeout.
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.