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 · Ontario, Canada
The Regulatory Strategy Senior Associate will develop regulatory pathways and support agency engagement planning for clinical development programs. They will also identify regulatory risks and opportunities while ensuring compliance and strategic alignment across cross-functional teams.
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 · Ontario, Canada
The consultant will provide technical support for regulatory publishing systems and document management technologies while troubleshooting complex issues. They will also partner with clients and internal teams to ensure effective system utilization and compliance with global submission standards.
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.
Remote · Ontario, Canada
The Site Activation Partner leads operational activities from study start-up to close-out to ensure compliance with timelines and regulatory standards. They coordinate essential document management, support site initiation, and maintain clinical trial systems to track site performance.
Remote · Alberta, Canada
The Site Activation Partner leads operational activities from study start-up to close-out to ensure compliance with timelines and regulatory standards. They coordinate essential document management, manage site initiation packages, and resolve investigator site issues to ensure successful trial activation.
Remote · United States
The Vice President of Commercial Strategy will drive new business growth by leading strategic market positioning and guiding high-impact bid pursuits. They will collaborate with cross-functional teams to analyze market opportunities and enhance Parexel's competitive advantage through effective sales messaging.
Remote · Ontario, Canada
The Study Operations Manager leads local study teams and oversees CROs to ensure operational delivery from study startup through close. Responsibilities include managing timelines, budgets, recruitment strategies, and regulatory submissions to Health Authorities and Ethics Committees.
Remote · Ontario, Canada
The Regulatory Strategy Senior Associate will develop regulatory pathway recommendations and support agency engagement planning for clinical products. They will also identify key regulatory risks and opportunities while ensuring compliance across cross-functional teams.
Remote · Canada, United States
The Global Study Manager II provides operational leadership throughout the clinical trial lifecycle, ensuring the execution of study management, site management, and vendor deliverables. They are responsible for driving study strategy, managing budgets, and overseeing cross-functional teams to ensure high-quality data delivery and inspection readiness.
Remote · Ontario, Canada
The Global Site Start-up Lead is responsible for the global execution and strategy of clinical trial site activation, ensuring compliance with SOPs and regulatory standards. They act as a subject matter expert, overseeing CRO performance and managing cross-functional team interactions to resolve site-related challenges.
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.
On-site
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Parexel FSP is looking for Regional Site Start Up II t…
Remote · Canada
The Local Study Associate Director leads local study teams to deliver clinical trials according to budget, timelines, and regulatory guidelines. They oversee site identification, monitoring activities, and ensure the completeness of essential trial documentation.
