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Parexel International Limited is a leading global biopharmaceutical services organization headquartered near Boston, Massachusetts, and in Durham, North Carolina. With over 16,000 employees and a presence in more than 100 countries, Parexel specializes in comprehensive drug development capabilities, including regulatory expertise, Phase I-IV clinical research services, and advanced commercialization solutions. The company is dedicated to improving global health by providing innovative clinical development solutions, underpinned by a strong commitment to empathy and making a difference in patients' lives. Parexel's collaborative approach fosters partnerships across various disciplines, ensuring high-quality scientific contributions and the successful delivery of epidemiology services and real-world studies.
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Parexel International
The Project Coordinator at Parexel is responsible for managing clinical projects and ensuring compliance while collaborating with various stakeholders.
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Parexel International
The Global Trial Manager will oversee clinical trials, ensuring compliance and effective management of CRO partners.
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Parexel International
Join Parexel as a Clinical Research Associate II/Senior CRA to manage and monitor clinical trials, ensuring patient safety and quality execution.
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Parexel International
Join Parexel as a Senior Machine Learning Engineer I to lead innovative AI-driven projects in the life sciences sector.
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Parexel International
The Senior Clinical Research Associate will ensure compliance and data integrity in clinical trials, primarily working remotely.
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Parexel International
Join Parexel as a Clinical Data Analyst I/II and contribute to clinical data cleaning and management in a global healthcare environment.
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Parexel International
The Regulatory Affairs Consultant is responsible for developing CMC strategies and managing regulatory submissions to ensure compliance with health authority guidelines.
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Parexel International
The Senior Clinical Research Associate is responsible for managing clinical studies and ensuring compliance with guidelines while collaborating with local teams.
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Parexel International
The Senior Regulatory Affairs Associate is responsible for managing life cycle maintenance and regulatory submissions across various international markets.
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Parexel International
Join Parexel as a Senior Statistical Programmer to enhance patient-reported outcomes in oncology through SAS programming.
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Parexel International
The Principal Statistical Programmer leads statistical programming efforts to support clinical trials at Parexel, ensuring high-quality deliverables and compliance with regulatory standards.
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Parexel International
Join Parexel as a Senior Clinical Research Associate I to manage oncology clinical sites in the Paris region.
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Parexel International
The Senior Regulatory Affairs Associate will manage regulatory submissions and compliance for drug products, ensuring adherence to global standards.
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Parexel International
The Senior Statistical Programmer at Parexel is responsible for leading statistical programming projects, ensuring quality and compliance in clinical trials.
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Parexel International
Join Parexel as a Senior Data Engineer to lead data management solutions for clinical trials, ensuring high-quality deliverables and project success.